Platinum compounds, compositions, and uses thereof

ABSTRACT

The present teachings relate to compounds and compositions for treatment of cancers. In some embodiments, the composition comprises a platinum (IV) complex having at least one reacting group for reacting with a functional group on a protein, engineered protein, antibody, antibody fragment, peptide, agonist, antagonist, aptamer or ligand which may be capable of recognizing a selected target cell population, and/or derivatives/analogs/mimics thereof.

REFERENCED TO RELATED APPLICATIONS

The present application is a continuation of U.S. application Ser. No.14/944,610 filed Nov. 18, 2015, entitled Platinum Compounds,Compositions, and Uses Thereof, which is a continuation of PCTApplication No. PCT/US15/37071 filed Jun. 23, 2015, entitled PlatinumCompounds, Compositions, and Uses Thereof, which claims priority to U.S.Provisional Patent Application No. 62/015,714, filed Jun. 23, 2014,entitled Monomaleimide Compounds, Compositions, and Uses Thereof, U.S.Provisional Patent Application No. 62/034,124, filed Aug. 6, 2014,entitled Monomaleimide Compounds, Compositions, and Uses Thereof, U.S.Provisional Patent Application No. 62/035,126, filed Aug. 8, 2014,entitled Novel Procedures of Synthesizing and Purifying PlatinumCompounds, U.S. Provisional Patent Application No. 62/035,739, filedAug. 11, 2014, entitled Novel Procedures of Synthesizing and PurifyingPlatinum Compounds, and U.S. Provisional Patent Application No.62/150,045, filed Apr. 20, 2015, entitled Platinum Compounds,Compositions, and Uses Thereof, the contents of each of which are hereinincorporated by reference in their entirety.

FIELD OF THE INVENTION

The invention relates to platinum based compounds.

BACKGROUND OF THE INVENTION

Platinum-based drugs are among the most active and widely usedanticancer agents. Cisplatin is one of the few FDA-approved,platinum-based cancer chemotherapeutics. Although cisplatin is effectiveagainst a number of solid tumors, especially testicular and ovariancancer, its clinical use has been limited because of its toxic effectsas well as the intrinsic and acquired resistance of some tumors to thisdrug.

To overcome these limitations, platinum analogs with lower toxicity andgreater activity in cisplatin-resistant tumors have been developed andtested, resulting in the approval of carboplatin and oxaliplatin in theUnited States. For example, carboplatin has the advantage of being lessnephrotoxic, but its cross-resistance with cisplatin has limited itsapplication in otherwise cisplatin-treatable diseases.

Oxaliplatin, however, exhibits a different anticancer spectrum from thatof cisplatin. It has been approved as the first or second line therapyin combination with 5-fluorouracil/leucovorin for advanced colorectalcancer, for which cisplatin and carboplatin are essentially inactive.These platinum drugs have platinum in the 2+ oxidative state (Pt(II))and are not orally active.

Platinum complexes in the 4+ oxidative state (Pt(IV) complexes) provideseveral advantages. Platinum(IV) complexes are substantially inactive inthe 4+ oxidation state but become activated upon reduction to theplatinum(II) state. As such Pt(IV) complexes constitute prodrugs ofPt(II) drugs that are activated in tumor cells. The two additionalcoordination sites (the axial sites) of Pt(IV) complexes can also bemodified to change the pharmacokinetic properties of the complexes.

The two axial sites, as well as the four equatorial sites, can include areacting group capable of reacting with amino groups, hydroxyl groups orthiol groups, forming a conjugate with a protein, antibody, antibodyfragment, peptide, agonist, antagonist, aptamer or ligand which may becapable of recognizing a selected target cell population. Theconjugation of the platinum(IV) complex can be performed prior toadministration or can take place in vivo. The benefits of theconjugation for the platinum (IV) complex include increased circulationtime, improved delivery to a target organ or to a targeted cellpopulation.

The inclusion of a reacting group as disclosed in the present teachingsmay increase the Pt concentration in tumor cells and, in certaininstances, may increase the efficacy in treating a disease or acondition discussed herein. In certain instances, Pt(IV) complexes ofthe present teachings can have a reduced long-term toxicity.

SUMMARY OF THE INVENTION

The present teachings relate to compositions, for example, for reducing,disrupting, or inhibiting the growth of a cancer cell or inducing thedeath of a cancer cell.

The composition can include a platinum (IV) compound. In variousembodiments, the platinum (IV) compound includes a suitable reactinggroup for reacting with a functional group on a protein, engineeredprotein, antibody, antibody fragment, peptide, agonist, antagonist,aptamer or ligand which may be capable of recognizing a selected targetcell population, and/or derivatives/analogs/mimics thereof. Suchcompounds are referred to herein as Pt(IV)M. The reacting group may be aMichael acceptor and/or alkylating functionality. For example, a Michaelacceptor can be introduced by a linker between platinum and the Michaelacceptor and/or alkylating functionality and/or alkylatingfunctionality. In various embodiments, one of or both the axialpositions of platinum each comprises one or more Michael acceptorsand/or alkylating functionality.

In some embodiments, the present teachings provide a compound of FormulaI:

or a pharmaceutically acceptable salt thereof, wherein:X and Y are independently selected from NH, alkyl and aryl;R¹ and R² each is Cl, or R¹ and R² are joined to form an oxalate;R³ is hydrogen, alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl,wherein each of the alkyl, alkenyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl groups optionally is substituted with one or more groups,each independently selected from halogen, cyano, nitro, hydroxyl,carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl, wherein each of the carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, or heterocyclyl is optionallysubstituted with one or more groups, each independently selected fromhalogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, heterocyclyl;R⁴ and R⁵ are each H or together constitute a cyclohexyl ring; andZ is alternatively absent, alkyl, aryl, cycloalkyl, heterocyclyl, aryl,and heteroaryl, wherein each of the alkyl, alkenyl, cycloalkyl,heterocyclyl, aryl, and heteroaryl groups optionally is substituted withone or more groups, each independently selected from halogen, cyano,nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino,amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl, or alkylidene hydrazine wherein each of thecarboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl or alkylidene hydrazine is optionally substituted with oneor more groups, each independently selected from halogen, cyano, nitro,hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide,carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl. R⁶ is a suitable reacting group for reacting afunctional group of a protein, engineered protein, antibody, antibodyfragment, peptide, agonist, antagonist, aptamer or ligand which may becapable of recognizing a selected target cell population, and/orderivatives/analogs/mimics thereof, and wherein R⁶ is selected from anyof the following groups:

where R⁷ is Cl, Br, F, mesylate, tosylate, O-(4-nitrophenyl),O-pentafluorophenyl. The reacting group can also comprise an activateddisulfide group, a vinylcarbonyl group, a vinyl acetylene group, anepoxide, an aziridine group or an acetylene group. The groups may besubstituted, where appropriate.

The present teachings also provide compositions including a compound asdescribed herein and methods of using a compound or a composition asdescribed herein. In various embodiments, the methods of the presentteachings are useful for the prevention or treatment of diseases thatbenefit from increased cell death or decreased cell proliferation. Forexample, the method of the present teachings can be used to increasecancer cell death or decrease cancer cell proliferation. The increasedcancer cell death or decreased cancer proliferation can occur, forexample, outside the body (in vitro) or inside the body (in vivo).

Certain embodiments of the present teachings also provide for use of acompound as described herein as a medicament for treating or preventinga disease and/or in the manufacture of such a medicament, e.g., for usein the treatment of a disease. Some embodiments provide the use of acompound as described herein for use as a medicament. In certainembodiments, the teachings provide a compound or composition asdescribed herein for the treatment of disease, e.g. for the treatment ofa cancer. In certain embodiments, the teachings provide a compound orcomposition as described herein for the treatment of a tumor, whereinthe tumor cells express one or more KRAS mutations.

The present teachings also provide a novel method of synthesizing andpurifying compounds as described herein.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a graph illustrating growth curves of A2780 tumors in nudemouse xenografts when mice were dosed with two control drugs, vehicle orthree Pt(IV)M of the present teachings.

FIG. 2 is a graph illustrating growth curves of A2780 tumors in nudemouse xenografts when the mice were dosed with two control drugs,vehicle or three Pt(IV)M of the present teachings.

FIG. 3 is a graph illustrating growth curves of A2780 tumors in nudemouse xenografts when the mice were dosed with two control drugs,vehicle or two Pt(IV)M of the present teachings.

FIG. 4 is a graph illustrating growth curves of A2780 tumors in nudemouse xenografts when the mice were dosed with two control drugs,vehicle or a Pt(IV)M of the present teachings.

FIG. 5 is a graph illustrating growth curves of Calu-6 tumors in nudemouse xenografts when the mice were dosed with two control drugs,vehicle or a Pt(IV)M of the present teachings.

FIG. 6 is a graph illustrating growth curves of A2780 tumors in nudemouse xenografts when the mice were dosed with two control drugs,vehicle or two Pt(IV)M of the present teachings.

FIG. 7 is a graph illustrating growth curves of Calu-6 tumors in nudemouse xenografts when the mice were dosed with two control drugs,vehicle or two Pt(IV)M of the present teachings.

FIG. 8 is a graph depicting platinum levels in tumor when platinum (IV)was dosed in the form of eight exemplary compounds of the presentteachings and two comparison compounds to tumor-bearing nude mice viaintravenous administration.

FIG. 9 is an liquid chromatography-inductively coupled plasma massspectrometry (LC-ICPMS) chromatogram showing the retention time of aPt(IV)M of the present teachings.

FIG. 10 is an LC-ICPMS chromatogram showing the retention time of aproduct of the incubation of a Pt(IV)M of the present teachings withcommercial albumin.

FIG. 11A is an LC-ICPMS chromatogram showing the retention time of aproduct of the incubation of a Pt(IV)M of the present teachings with ratserum. FIG. 11B is LC MS/MS analysis of a Pt(IV)M of the presentteachings with albumin tryptic peptide T3.

FIG. 12 is a graph illustrating growth curves of KRAS mutant Calu-6tumors when the mice were dosed with a control drug, vehicle or aPt(IV)M of the present teachings.

FIG. 13 is a graph illustrating albumin uptake in KRAS mutant cells andKRAS WT cells in vitro.

FIG. 14 shows uptake of fluorescently labeled albumin in KRAS mutantcells and KRAS WT cells in vitro.

FIG. 15 is a graph illustrating growth curves of KRAS wild type BxPC-3pancreatic cancer model when the mice were dosed with a control drug,vehicle or a Pt(IV)M of the present teachings.

FIG. 16 is a graph illustrating growth curves of KRAS mutant Miapaca-2pancreatic cancer model when the mice were dosed with a control drug,vehicle or a Pt(IV)M of the present teachings.

FIG. 17 shows TGI % of cisplatin, oxaliplatin, bismaleimide compoundsand Pt(IV)M monomaleimide compounds.

FIG. 18 shows platinum accumulation in plasma and tumor with a singledose of a Pt(IV)M monomaleimide compound and cisplatin in lung cancermodel NCI-H460.

FIG. 19 shows platinum accumulation and DNA platination in plasma andtumor with two doses of a Pt(IV)M monomaleimide compound and cisplatinin lung cancer model NCI-H520.

FIG. 20 compares tumor volume in ovarian cancer model A2780 withtreatment with cisplatin and a Pt(IV)M monomaleimide compound.

FIG. 21 shows post-studt platinum levels in ovarian cancer model A2780with treatment with cisplatin and a Pt(IV)M monomaleimide compound.

FIG. 22 compares tumor volume after multiple doses of cisplatin and aPt(IV)M monomaleimide compound in lung cancer model NCI-H520 for 32days.

FIG. 23 shows platinum levels after multiple doses of cisplatin and aPt(IV)M monomaleimide compound in lung cancer model NCI-H520 for 32days.

FIG. 24 shows cell dedifferentiation images from day 10 of NCI-H520study.

FIG. 25 shows TUNEL apoptosis images from day 10 of NCI-H520 study.

FIG. 26 shows platinum concentrations in rats over a period of up to 100hours after treatment with cisplatin and a Pt(IV)M monomaleimidecompound.

FIG. 27 shows platinum concentrations in dogs over a period of up to 400hours after treatment with cisplatin and a Pt(IV)M monomaleimidecompound.

FIG. 28 shows RBC partitioning and protein partitioning after treatmentwith a Pt(IV)M monomaleimide compound.

FIG. 29 shows platinum concentrations in plasma in rats treated with aPt(IV)M compound in direct infusion or pre-conjugated to albumin.

FIG. 30 shows average tumor volumes and platinum levels in the tumors inMX-1 breast cancer model treated with cisplatin and a Pt(IV)Mmonomaleimide compound.

FIG. 31 shows levels of blood markers of kidney damage after treatmentswith cisplatin and a Pt(IV)M monomaleimide compound.

DETAILED DESCRIPTION

Applicants have discovered that Pt(IV) compounds having a suitablereacting group for reacting with a functional group on a protein,engineered protein, antibody, antibody fragment, peptide, agonist,antagonist, aptamer or ligand which may be capable of recognizing aselected target cell population, and/or derivatives/analogs/mimicsthereof, are effective inhibitors of cellular proliferation and tumorgrowth. Such compounds are referred to herein as Pt(IV)M compounds. Theproduct resulting from the reaction of Pt(IV)M with a functional grouppresent on either a protein, engineered protein, antibody, antibodyfragment, peptide, agonist, antagonist, aptamer or ligand are referredto herein as Pt(IV)M conjugates.

The term “ligand” as used herein includes any molecule that specificallybinds or reactively associated or complexes with a receptor or otherreceptive moiety associated with a given target cell population.

The term “reacting group” as used herein refers to a functional group ofthe Pt(IV) compounds that may react with a functional group on aprotein, engineered protein, antibody, antibody fragment, peptide,agonist, antagonist, aptamer or ligand which may be capable ofrecognizing a selected target cell population, and/orderivatives/analogs/mimics thereof. The functional group on a protein,engineered protein, antibody, antibody fragment, peptide, agonist,antagonist, aptamer or ligand which may be capable of recognizing aselected target cell population, and/or derivatives/analogs/mimicsthereof, may be amino groups, hydroxyl groups or thiol groups.

Non-limiting examples of a reacting group include an activated disulfidegroup, a vinylcarbonyl group, a vinyl acetylene group, an epoxide, anaziridine group or an acetylene group. The groups may be substituted,where appropriate. The reacting group may also be any of:

where R⁷ is Cl, Br, F, mesylate, tosylate, O-(4-nitrophenyl),O-pentafluorophenyl.

In some embodiments, the Pt(IV)M conjugate results from the reaction ofthe Pt(IV)M compound with the protein, engineered protein, antibody,antibody fragment, peptide, agonist, antagonist, aptamer or ligand whichmay be capable of recognizing a selected target cell population, and/orderivatives/analogs/mimics thereof, in vivo, i.e., the conjugationbetween the reacting group and the functional group takes place in vivo.

In some embodiments, Pt(IV)M conjugate results from the reaction of thePt(IV)M compound with the protein, engineered protein, antibody,antibody fragment, peptide, agonist, antagonist, aptamer or ligand whichmay be capable of recognizing a selected target cell population, and/orderivatives/analogs/mimics thereof, prior to administration outside ofthe body, i.e., the conjugation between the reacting group and thefunctional group is performed prior to administration in vivo.

The protein, engineered protein, antibody, antibody fragment, peptide,agonist, antagonist, aptamer or ligand which may be capable ofrecognizing a selected target cell population, and/orderivatives/analogs/mimics thereof may be any ligand disclosed in EP0554708 to Willner et al. (BMS), the contents of which are incorporatedherein by reference in their entirety. For example, the protein,engineered protein, antibody, antibody fragment, peptide, agonist,antagonist, aptamer or ligand which may be capable of recognizing aselected target cell population, and/or derivatives/analogs/mimicsthereof may be non-immunoreactive, such as but not limited totransferrin, epidermal growth factors (“EGF”), bombesin, gastrin,gastrin-releasing peptide, platelet-derived growth factor, IL-2, IL-6,tumor growth factors (“TGF”), such as TGF-α and TGF-β, vaccinia growthfactor (“VGF”), insulin and insulin-like growth factors I and II.Non-peptidyl ligands may include, for example, steroids, carbohydratesand lectins. The protein, engineered protein, antibody, antibodyfragment, peptide, agonist, antagonist, aptamer or ligand which may becapable of recognizing a selected target cell population, and/orderivatives/analogs/mimics thereof may also be non-immunoreactive suchas but not limited to an antigen-recognizing immunoglobulin (alsoreferred to as “antibody”), or antigen-recognizing fragment thereof. Theimmunoglobulins may be immunoglobulins which can recognize atumor-associated antigen. As used, “immunoglobulin” may refer to anyrecognized class or subclass of immunoglobulins such as IgG, IgA, IgM,IgD, or IgE. The immunoglobulin can be derived from any species such ashuman, murine, or rabbit origin. Further, the immunoglobulin may bepolyclonal, monoclonal, chimeric, bifunctional or hybrid.

In some embodiments, the protein is albumin orderivatives/analogs/mimics thereof. In some embodiments, the engineeredprotein may be a recombinant albumin (rAlbumin) such as the recombinantalbumin disclosed in US 20090280534 to Christensen et al. (Novozymes),the contents of which are incorporated herein by reference in theirentirety.

The reacting group may be a Michael acceptor and/or alkylatingfunctionality. In some embodiments, the Pt(IV)M compounds comprise amaleimide group and/or derivatives thereof.

“Michael acceptor”, as used herein, refers to an α,β-unsaturatedelectrophile, such as, but not limited to, an α,β-un saturated carbonylderivative or an α,β-unsaturated nitrile: “Electrophile” means able toaccept an electron pair; “α,β-unsaturated electrophile” means thecompound class that includes, but is not limited to, α,β-unsaturatedcarbonyl derivative, α,β-unsaturated nitrile, α,β-unsaturated sulfone,or other vinyl derivative substituted with a strong electron withdrawinggroup, such as, but not limited to, a nitro group; “α,β-unsaturatedcarbonyl derivative” means the compound class that includes, but is notlimited to, α,β-unsaturated ketone, quinone or derivative thereof,α,β-unsaturated aldehyde, α,β-unsaturated carboxylic acid derivative,such as, but not limited to, an ester, an amide, a substituted amide, ora maleimide or a derivative thereof.

A feature of the Pt(IV)M compounds and/or Pt(IV)M conjugates is theirrelatively low toxicity to an organism while maintaining efficacy atinhibiting, e.g. slowing or stopping tumor growth. As used herein,“toxicity” refers to the capacity of a substance or composition to beharmful or poisonous to a cell, tissue organism or cellular environment.Low toxicity refers to a reduced capacity of a substance or compositionto be harmful or poisonous to a cell, tissue organism or cellularenvironment. Such reduced or low toxicity may be relative to a standardmeasure, relative to a treatment or relative to the absence of atreatment.

Toxicity may further be measured relative to a subject's weight losswhere weight loss over 15%, over 20% or over 30% of the body weight isindicative of toxicity. Other metrics of toxicity may also be measuredsuch as patient presentation metrics including lethargy and generalmalaise. Neutropenia or thrombopenia may also be metrics of toxicity.

Pharmacologic indicators of toxicity include elevated AST/ALT levels,neurotoxicity, kidney damage, GI damage and the like.

Furthermore, in some embodiments, such Pt(IV)M compounds and/or Pt(IV)Mconjugates are effective for inhibiting tumor growth, whether measuredas a net value of size (weight, surface area or volume) or as a rateover time, in multiple types of tumors.

In some embodiments the size of a tumor is reduced by 60% or more. Insome embodiments, the size of a tumor is reduced by at least 20%, atleast 30%, at least 40%, at least 50%, at least 60%, at least 70%, atleast 80%, at least 90%, at least 95%, at least 96%, at least 97%, atleast 98%, at least 99%, at least 100%, by a measure of weight, and/orarea and/or volume.

In some embodiments, the RECIST (Response Evaluation Criteria In SolidTumors) criteria are used to characterize the effects of the compoundsof the invention on solid tumors. The guidelines for gauging tumors wereupdated and published in the European Journal of Cancer (EJC) in January2009 (Eisenhauer, et al., European Journal of Cancer: 45 (2009)228-247), the contents of which are incorporated herein by reference intheir entirety. Any of the RECIST metrics may be used to characterizethe effects of the compounds of the invention on tumors including butnot limited to response, assessment and measurement criteria.

In some embodiments Progression Free Survival and Overall Survival areused to characterize the effects of the compounds of the invention onsolid tumors.

It has been surprisingly found that the relative ability of Pt(IV)Mcompounds and/or Pt(IV)M conjugates of the invention to inhibit in vitrocell proliferation is not predictive of their relative ability toinhibit tumor growth, i.e., their relative ability to inhibit tumorgrowth is greater than their relative ability to inhibit cellproliferation in vitro.

Without wishing to be bound to any theory, the effective delivery of aPt(IV)M compound may be related to the covalent attachment of thecompound to a protein such as albumin. Conjugation to albumin preventsrapid clearance and delivers stable and inactive form of platinum totumor sites. The compound-albumin bond may be cleaved at a tumor site,creating an active platinum compound, e.g., a Pt(II) compound.Trafficking of a Pt(IV)M compound by albumin is being studied with MIAPaCa-2 and BxPC-3 cell lines (Commisso et al., Nature, vol. 497:633-637(2013), the contents of which are incorporated herein by reference intheir entirety).

In some embodiments, a Pt(IV)M compound and/or Pt(IV)M conjugates asdescribed herein is administered to a subject who has a tumor comprisingcells that express one or more KRAS mutations. A subject's tumor may beassayed for KRAS mutations using methods known in the art, for example,see Anderson, 2011, Expert Rev Mol Diagn. 11:635-642 and Thierry et al.,2014, Nature Medicine 20:430-435, the contents of each of which areincorporated herein by reference in their entirety. If the tumor has aKRAS mutation, the tumor is likely to be responsive to treatment by thePt(IV)M compounds and/or Pt(IV)M conjugates disclosed herein. In someembodiments, the tumor is directly assayed for the presence of a KRASmutation. In some embodiments, a non-tumor tissue, e.g., tumor DNA thatis circulating in the plasma is assayed for the presence of a KRASmutation.

This finding is also important because some tumors containing cells thatexpress one or more KRAS mutants are not sensitive to certaintreatments. For example, colorectal cancer patients are tested for thepresence of KRAS mutations because the presence of certain of thesemutations predicts resistance to therapies directed against EGFR (Sienaet al., 2009, J Natl Cancer Inst 101:1308-24, the contents of which areincorporated herein by reference in their entirety). Such patients arecandidates for treatments with a Pt(IV)M compound and/or Pt(IV)Mconjugates described herein.

For convenience, before further description of the present teachings,certain definitions of terms employed in the specification and claimsare collected here. These definitions should be read in light of theremainder of the disclosure and as understood by a person of ordinaryskill in the art. Unless defined otherwise, all technical and scientificterms used herein have the same meaning as commonly understood by aperson of ordinary skill in the art.

The articles “a” and “an,” as used herein, should be understood to mean“at least one,” unless clearly indicated to the contrary.

The phrase “and/or,” as used herein, should be understood to mean“either or both” of the elements so conjoined, i.e., elements that areconjunctively present in some cases and disjunctively present in othercases. Other elements may optionally be present other than the elementsspecifically identified by the “and/or” clause, whether related orunrelated to those elements specifically identified unless clearlyindicated to the contrary. Thus, as a non-limiting example, a referenceto “A and/or B,” when used in conjunction with open-ended language suchas “comprising” can refer, in one embodiment, to A without B (optionallyincluding elements other than B); in another embodiment, to B without A(optionally including elements other than A); in yet another embodiment,to both A and B (optionally including other elements).

As used herein, “or” should be understood to have the same meaning as“and/or” as defined above. For example, when separating items in a list,“or” or “and/or” shall be interpreted as being inclusive, i.e., theinclusion of at least one, but also including more than one, of a numberor list of elements, and, optionally, additional unlisted items. Onlyterms clearly indicated to the contrary, such as “only one of” or“exactly one of,” or, when used in the claims, “consisting of,” willrefer to the inclusion of exactly one element of a number or list ofelements.

In general, the term “or” as used herein shall only be interpreted asindicating exclusive alternatives (i.e. “one or the other but not both”)when preceded by terms of exclusivity, such as “either,” “one of” “onlyone of” or “exactly one of” “Consisting essentially of,” when used inthe claims, shall have its ordinary meaning as used in the field ofpatent law.

As used herein, the phrase “at least one” in reference to a list of oneor more elements should be understood to mean at least one elementselected from any one or more of the elements in the list of elements,but not necessarily including at least one of each and every elementspecifically listed within the list of elements and not excluding anycombinations of elements in the list of elements. This definition alsoallows that elements may optionally be present other than the elementsspecifically identified within the list of elements to which the phrase“at least one” refers, whether related or unrelated to those elementsspecifically identified.

Thus, as a non-limiting example, “at least one of A and B” (or,equivalently, “at least one of A or B,” or, equivalently “at least oneof A and/or B”) can refer, in one embodiment, to at least one,optionally including more than one, A, with no B present (and optionallyincluding elements other than B); in another embodiment, to at leastone, optionally including more than one, B, with no A present (andoptionally including elements other than A); in yet another embodiment,to at least one, optionally including more than one, A, and at leastone, optionally including more than one, B (and optionally includingother elements); etc.

As used herein, all transitional phrases such as “comprising,”“including,” “carrying,” “having,” “containing,” “involving,” “holding,”and the like are to be understood to be open-ended, i.e., to meanincluding but not limited to.

Only the transitional phrases “consisting of” and “consistingessentially of” shall be closed or semi-closed transitional phrases,respectively, as set forth in the United States Patent Office Manual ofPatent Examining Procedures.

As used herein, a “subject” or a “patient” refers to any mammal (e.g., ahuman), such as a mammal that may be susceptible to a disease ordisorder, for example, tumorigenesis or cancer. Examples include ahuman, a non-human primate, a cow, a horse, a pig, a sheep, a goat, adog, a cat, or a rodent such as a mouse, a rat, a hamster, or a guineapig. In various embodiments, a subject refers to one that has been orwill be the object of treatment, observation, or experiment. Forexample, a subject can be a subject diagnosed with cancer or otherwiseknown to have cancer or one selected for treatment, observation, orexperiment on the basis of a known cancer in the subject.

As used herein, “treatment” or “treating” refers to amelioration of adisease or disorder, or at least one sign or symptom thereof “Treatment”or “treating” can refer to reducing the progression of a disease ordisorder, as determined by, e.g., stabilization of at least one sign orsymptom or a reduction in the rate of progression as determined by areduction in the rate of progression of at least one sign or symptom. Inanother embodiment, “treatment” or “treating” refers to delaying theonset of a disease or disorder.

As used herein, “prevention” or “preventing” refers to a reduction ofthe risk of acquiring or having a sign or symptom a given disease ordisorder, i.e., prophylactic treatment.

The phrase “therapeutically effective amount” as used herein means thatamount of a compound, material, or composition comprising a compound ofthe present teachings that is effective for producing a desiredtherapeutic effect. Accordingly, a therapeutically effective amounttreats or prevents a disease or a disorder, e.g., ameliorates at leastone sign or symptom of the disorder. In various embodiments, the diseaseor disorder is a cancer.

A dash (“-”) that is not between two letters or symbols is used toindicate a point of attachment for a substituent. For example, —CONH₂ isattached through the carbon atom (C).

By “optional” or “optionally,” it is meant that the subsequentlydescribed event or circumstance may or may not occur, and that thedescription includes instances where the event or circumstance occursand instances in which it does not. For example, “optionally substitutedaryl” encompasses both “aryl” and “substituted aryl” as defined herein.It will be understood by those ordinarily skilled in the art, withrespect to any group containing one or more substituents, that suchgroups are not intended to introduce any substitution or substitutionpatterns that are sterically impractical, synthetically non-feasible,and/or inherently unstable.

The term “alkyl” as used herein refers to a saturated straight orbranched hydrocarbon, such as a straight or branched group of 1-22, 1-8,1-6, or 1-4 carbon atoms, referred to herein as (C₁-C₂₂)alkyl,(C₁-C₈)alkyl, (C₁-C₆)alkyl, and (C₁-C₄)alkyl, respectively. Exemplaryalkyl groups include, but are not limited to, methyl, ethyl, propyl,isopropyl, 2-methyl-1-propyl, 2-methyl-2-propyl, 2-methyl-1-butyl,3-methyl-1-butyl, 2-methyl-3-butyl, 2,2-dimethyl-1-propyl,2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl,2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl,2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, butyl,isobutyl, t-butyl, pentyl, isopentyl, neopentyl, hexyl, heptyl, andoctyl.

The term “alkenyl” as used herein refers to an unsaturated straight orbranched hydrocarbon having at least one carbon-carbon double bond(shown, for example, as “═”), such as a straight or branched group of2-22, 2-8, 2-6, or 2-4 carbon atoms, referred to herein as(C₂-C₂₂)alkenyl, (C₂-C₈)alkenyl, (C₂-C₆)alkenyl, and (C₂-C₄)alkenyl,respectively. Exemplary alkenyl groups include, but are not limited to,vinyl, allyl, butenyl, pentenyl, hexenyl, butadienyl, pentadienyl,hexadienyl, 2-ethylhexenyl, 2-propyl-2-butenyl, and4-(2-methyl-3-butene)-pentenyl.

The term “alkynyl” as used herein refers to an unsaturated straight orbranched hydrocarbon having at least one carbon-carbon triple bond(shown, for example, as “≡”), such as a straight or branched group of2-22, 2-8, 2-6, 2-4 carbon atoms, referred to herein as (C₂-C₂₂)alkynyl,(C₂-C₈)alkynyl, (C₂-C₆)alkynyl, and (C₂-C₄)alkynyl, respectively.Exemplary alkynyl groups include, but are not limited to, ethynyl,propynyl, butynyl, pentynyl, hexynyl, methylpropynyl,4-methyl-1-butynyl, 4-propyl-2-pentynyl, and 4-butyl-2-hexynyl.

The term “cycloalkyl” as used herein refers to a saturated orunsaturated monocyclic, bicyclic, other multicyclic, or bridged cyclichydrocarbon group. A cycloalkyl group can have 3-22, 3-12, or 3-8 ringcarbons, referred to herein as (C₃-C₂₂)cycloalkyl, (C₃-C₁₂)cycloalkyl,or (C₃-C₈)cycloalkyl, respectively. A cycloalkyl group can also have oneor more carbon-carbon double bond or carbon-carbon triple bond.

Exemplary monocyclic cycloalkyl groups include, but are not limited to,cyclopentanes (cyclopentyls), cyclopentenes (cyclopentenyls),cyclohexanes (cyclohexyls), cyclohexenes (cyclopexenyls), cycloheptanes(cycloheptyls), cycloheptenes (cycloheptenyls), cyclooctanes(cyclooctyls), cyclooctenes (cyclooctenyls), cyclononanes (cyclononyls),cyclononenes (cyclononenyls), cyclodecanes (cyclodecyls), cyclodecenes(cyclodecenyls), cycloundecanes (cycloundecyls), cycloundecenes(cycloundecenyls), cyclododecanes (cyclododecyls), and cyclododecenes(cyclododecenyls). Other exemplary cycloalkyl groups, includingbicyclic, multicyclic, and bridged cyclic groups, include, but are notlimited to, bicyclobutanes (bicyclobutyls), bicyclopentanes(bicyclopentyls), bicyclohexanes (bicyclohexyls), bicycleheptanes(bicycloheptyls, including bicyclo[2,2,1]heptanes(bicycle[2,2,1]heptyls) and bicycle[3,2,0]heptanes(bicycle[3,2,0]heptyls)), bicyclooctanes (bicyclooctyls, includingoctahydropentalene (octahydropentalenyl), bicycle[3,2,1]octane(bicycle[3,2,1]octyl), and bicylo[2,2,2]octane (bicycle[2,2,2]octyl)),and adamantanes (adamantyls). Cycloalkyl groups can be fused to othercycloalkyl saturated or unsaturated, aryl, or heterocyclyl groups.

The term “aryl” as used herein refers to a mono-, bi-, or othermulti-carbocyclic aromatic ring system. The aryl can have 6-22, 6-18,6-14, or 6-10 carbons, referred to herein as (C₆-C₂₂)aryl, (C₆-C₁₈)aryl,(C₆-C₁₄)aryl, or (C₆-C₁₀)aryl, respectively. The aryl group canoptionally be fused to one or more rings selected from aryls,cycloalkyls, and heterocyclyls. The term “bicyclic aryl” as used hereinrefers to an aryl group fused to another aromatic or non-aromaticcarbocylic or heterocyclic ring. Exemplary aryl groups include, but arenot limited to, phenyl, tolyl, anthracenyl, fluorenyl, indenyl,azulenyl, and naphthyl, as well as benzo-fused carbocyclic moieties suchas 5,6,7,8-tetrahydronaphthyl. Exemplary aryl groups also include, butare not limited to a monocyclic aromatic ring system, wherein the ringcomprises 6 carbon atoms, referred to herein as “(C₆)aryl” or phenyl.The phenyl group can also be fused to a cyclohexane or cyclopentane ringto form another aryl.

The term “arylalkyl” as used herein refers to an alkyl group having atleast one aryl substituent (e.g., -aryl-alkyl-). Exemplary arylalkylgroups include, but are not limited to, arylalkyls having a monocyclicaromatic ring system, wherein the ring comprises 6 carbon atoms,referred to herein as “(C₆)arylalkyl.” The term “benzyl” as used hereinrefers to the group —CH₂-phenyl.

The term “heteroalkyl” refers to an alkyl group as described herein inwhich one or more carbon atoms is replaced by a heteroatom. Suitableheteroatoms include oxygen, sulfur, nitrogen, phosphorus, and the like.Examples of heteroalkyl groups include, but are not limited to, alkoxy,amino, thioester, and the like.

The terms “heteroalkenyl” and “heteroalkynyl” refer to unsaturatedaliphatic groups analogous in length and possible substitution to theheteroalkyls described above, but that contain at least one double ortriple bond, respectively.

The term “heterocycle” refers to cyclic groups containing at least oneheteroatom as a ring atom, in some cases, 1 to 3 heteroatoms as ringatoms, with the remainder of the ring atoms being carbon atoms. Suitableheteroatoms include oxygen, sulfur, nitrogen, phosphorus, and the like.In some cases, the heterocycle may be 3- to 10-membered ring structuresor 3- to 7-membered rings, whose ring structures include one to fourheteroatoms. The term “heterocycle” may include heteroaryl groups,saturated heterocycles (e.g., cycloheteroalkyl) groups, or combinationsthereof. The heterocycle may be a saturated molecule, or may compriseone or more double bonds. In some case, the heterocycle is a nitrogenheterocycle, wherein at least one ring comprises at least one nitrogenring atom. The heterocycles may be fused to other rings to form apolycylic heterocycle. Thus, heterocycles also include bicyclic,tricyclic, and tetracyclic groups in which any of the above heterocyclicrings is fused to one or two rings independently selected from aryls,cycloalkyls, and heterocycles. The heterocycle may also be fused to aspirocyclic group.

Heterocycles include, for example, thiophene, benzothiophene,thianthrene, furan, tetrahydrofuran, pyran, isobenzofuran, chromene,xanthene, phenoxathiin, pyrrole, dihydropyrrole, pyrrolidine, imidazole,pyrazole, pyrazine, isothiazole, isoxazole, pyridine, pyrazine,pyrimidine, pyridazine, indolizine, isoindole, indole, indazole, purine,quinolizine, isoquinoline, quinoline, phthalazine, naphthyridine,quinoxaline, quinazoline, cinnoline, pteridine, carbazole, carboline,triazole, tetrazole, oxazole, isoxazole, thiazole, isothiazole,phenanthridine, acridine, pyrimidine, phenanthroline, phenazine,phenarsazine, phenothiazine, furazan, phenoxazine, pyrrolidine, oxolane,thiolane, oxazole, oxazine, piperidine, homopiperidine(hexamethyleneimine), piperazine (e.g., N-methyl piperazine),morpholine, lactones, lactams such as azetidinones and pyrrolidinones,sultams, sultones, other saturated and/or unsaturated derivativesthereof, and the like.

In some cases, the heterocycle may be bonded to a compound via aheteroatom ring atom (e.g., nitrogen). In some cases, the heterocyclemay be bonded to a compound via a carbon ring atom. In some cases, theheterocycle is pyridine, imidazole, pyrazine, pyrimidine, pyridazine,acridine, acridin-9-amine, bipyridine, naphthyridine, quinoline,isoquinoline, benzoquinoline, benzoisoquinoline,phenanthridine-1,9-diamine, or the like.

The term “heteroaromatic” or “heteroaryl” as used herein refers to amono-, bi-, or multi-cyclic aromatic ring system containing one or moreheteroatoms, for example 1-3 heteroatoms, such as nitrogen, oxygen, andsulfur. Heteroaryls can also be fused to non-aromatic rings. In variousembodiments, the term “heteroaromatic” or “heteroaryl,” as used hereinexcept where noted, represents a stable 5- to 7-membered monocyclic,stable 9- to 10-membered fused bicyclic, or stable 12- to 14-memberedfused tricyclic heterocyclic ring system which contains an aromatic ringthat contains at least one heteroatom selected from the group consistingof N, O, and S. In some embodiments, at least one nitrogen is in thearomatic ring.

Heteroaromatics or heteroaryls can include, but are not limited to, amonocyclic aromatic ring, wherein the ring comprises 2-5 carbon atomsand 1-3 heteroatoms, referred to herein as “(C₂-C₅)heteroaryl.”Illustrative examples of monocyclic heteroaromatic (or heteroaryl)include, but are not limited to, pyridine (pyridinyl), pyridazine(pyridazinyl), pyrimidine (pyrimidyl), pyrazine (pyrazyl), triazine(triazinyl), pyrrole (pyrrolyl), pyrazole (pyrazolyl), imidazole(imidazolyl), (1,2,3)- and (1,2,4)-triazole ((1,2,3)- and(1,2,4)-triazolyl), pyrazine (pyrazinyl), pyrimidine (pyrimidinyl),tetrazole (tetrazolyl), furan (furyl), thiophene (thienyl), isoxazole(isoxazolyl), thiazole (thiazolyl), isoxazole (isoxazolyl), and oxazole(oxazolyl).

The term “bicyclic heteroaromatic” or “bicyclic heteroaryl” as usedherein refers to a heteroaryl group fused to another aromatic ornon-aromatic carbocylic or heterocyclic ring. Exemplary bicyclicheteroaromatics or heteroaryls include, but are not limited to 5,6- or6,6-fused systems, wherein one or both rings contain heteroatoms. Theterm “bicyclic heteroaromatic” or “bicyclic heteroaryl” also encompassesreduced or partly reduced forms of fused aromatic system wherein one orboth rings contain ring heteroatoms. The ring system may contain up tothree heteroatoms, independently selected from oxygen, nitrogen, andsulfur.

Exemplary bicyclic heteroaromatics (or heteroaryls) include, but are notlimited to, quinazoline (quinazolinyl), benzoxazole (benzoxazolyl),benzothiophene (benzothiophenyl), benzoxazole (benzoxazolyl),benzisoxazole (benzisoxazolyl), benzimidazole (benzimidazolyl),benzothiazole (benzothiazolyl), benzofurane (benzofuranyl),benzisothiazole (benzisothiazolyl), indole (indolyl), indazole(indazolyl), indolizine (indolizinyl), quinoline (quinolinyl),isoquinoline (isoquinolinyl), naphthyridine (naphthyridyl), phthalazine(phthalazinyl), phthalazine (phthalazinyl), pteridine (pteridinyl),purine (purinyl), benzotriazole (benzotriazolyl), and benzofurane(benzofuranyl). In some embodiments, the bicyclic heteroaromatic (orbicyclic heteroaryl) is selected from quinazoline (quinazolinyl),benzimidazole (benzimidazolyl), benzothiazole (benzothiazolyl), indole(indolyl), quinoline (quinolinyl), isoquinoline (isoquinolinyl), andphthalazine (phthalazinyl). In certain embodiments, the bicyclicheteroaromatic (or bicyclic heteroaryl) is quinoline (quinolinyl) orisoquinoline (isoquinolinyl).

The term “tricyclic heteroaromatic” or “tricyclic heteroaryl” as usedherein refers to a bicyclic heteroaryl group fused to another aromaticor non-aromatic carbocylic or heterocyclic ring. The term “tricyclicheteroaromatic” or “tricyclic heteroaryl” also encompasses reduced orpartly reduced forms of fused aromatic system wherein one or both ringscontain ring heteroatoms. Each of the ring in the tricyclicheteroaromatic (tricyclic heteroaryl) may contain up to threeheteroatoms, independently selected from oxygen, nitrogen, and sulfur.

Exemplary tricyclic heteroaromatics (or heteroaryls) include, but arenot limited to, acridine (acridinyl), 9H-pyrido[3,4-b]indole(9H-pyrido[3,4-b]indolyl), phenanthridine (phenanthridinyl),pyrido[1,2-a]benzimidazole (pyrido[1,2-a]benzimidazolyl), andpyrido[1,2-b]indazole (pyrido[1,2-b]indazolyl).

The term “alkoxy” as used herein refers to an alkyl group attached to anoxygen (—O-alkyl-). “Alkoxy” groups also include an alkenyl groupattached to an oxygen (“alkenyloxy”) or an alkynyl group attached to anoxygen (“alkynyloxy”) groups. Exemplary alkoxy groups include, but arenot limited to, groups with an alkyl, alkenyl or alkynyl group of 1-22,1-8, or 1-6 carbon atoms, referred to herein as (C₁-C₂₂)alkoxy,(C₁-C₈)alkoxy, or (C₁-C₆)alkoxy, respectively. Exemplary alkoxy groupsinclude, but are not limited to methoxy and ethoxy.

The term “cycloalkoxy” as used herein refers to a cycloalkyl groupattached to an oxygen.

The term “aryloxy” or “aroxy” as used herein refers to an aryl groupattached to an oxygen atom. Exemplary aryloxy groups include, but arenot limited to, aryloxys having a monocyclic aromatic ring system,wherein the ring comprises 6 carbon atoms, referred to herein as“(C₆)aryloxy.” The term “arylalkoxy” as used herein refers to anarylalkyl group attached to an oxygen atom. An exemplary aryalkyl groupis benzyloxy group.

The term “amine” or “amino” as used herein refers to both unsubstitutedand substituted amines, e.g., NR_(a)R_(b)R_(b′), where R_(a), R_(b), andR_(b′) are independently selected from alkyl, alkenyl, alkynyl, aryl,arylalkyl, carbamate, cycloalkyl, haloalkyl, heteroaryl, heterocyclyl,and hydrogen, and at least one of the R_(a), R_(b), and R_(b′) is nothydrogen. The amine or amino can be attached to the parent moleculargroup through the nitrogen. The amine or amino also may be cyclic, forexample any two of R_(a), R_(b), and R_(b′) may be joined togetherand/or with the N to form a 3- to 12-membered ring (e.g., morpholino orpiperidinyl). The term amino also includes the corresponding quaternaryammonium salt of any amino group. Exemplary amines include alkylamine,wherein at least one of R_(a)R_(b), or R_(b′) is an alkyl group, orcycloalkylamine, wherein at least one of R_(a)R_(b), or R_(b′) is acycloalkyl group.

The term “ammonia” as used herein refers to NH₃.

The term “aldehyde” or “formyl” as used herein refers to —CHO.

The term “acyl” term as used herein refers to a carbonyl radicalattached to an alkyl, alkenyl, alkynyl, cycloalkyl, heterocycyl, aryl,or heteroaryl. Exemplary acyl groups include, but are not limited to,acetyl, formyl, propionyl, benzoyl, and the like.

The term “amide” as used herein refers to the form —NR_(c)C(O)(R_(d))—or —C(O)NR_(c)R_(e), wherein R_(c), R_(d), and R_(e) are eachindependently selected from alkyl, alkenyl, alkynyl, aryl, arylalkyl,cycloalkyl, haloalkyl, heteroaryl, heterocyclyl, and hydrogen. The amidecan be attached to another group through the carbon, the nitrogen,R_(c), R_(d), or R_(e). The amide also may be cyclic, for example R_(c)and R_(e), may be joined to form a 3- to 12-membered ring, such as a 3-to 10-membered ring or a 5- or 6-membered ring. The term “amide”encompasses groups such as sulfonamide, urea, ureido, carbamate,carbamic acid, and cyclic versions thereof. The term “amide” alsoencompasses an amide group attached to a carboxy group, e.g.,-amide-COOH or salts such as -amide-COONa.

The term “arylthio” as used herein refers to an aryl group attached toan sulfur atom. Exemplary arylthio groups include, but are not limitedto, arylthios having a monocyclic aromatic ring system, wherein the ringcomprises 6 carbon atoms, referred to herein as “(C₆)arylthio.”

The term “arylsulfonyl” as used herein refers to an aryl group attachedto a sulfonyl group, e.g., —S(O)₂-aryl-. Exemplary arylsulfonyl groupsinclude, but are not limited to, arylsulfonyls having a monocyclicaromatic ring system, wherein the ring comprises 6 carbon atoms,referred to herein as “(C₆)arylsulfonyl.”

The term “carbamate” as used herein refers to the form—R_(f)OC(O)N(R_(g))—, —R_(f)OC(O)N(R_(g))R_(h)—, or —OC(O)NR_(g)R_(h),wherein R_(f), R_(g), and R_(h) are each independently selected fromalkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, haloalkyl,heteroaryl, heterocyclyl, and hydrogen. Exemplary carbamates include,but are not limited to, arylcarbamates or heteroaryl carbamates (e.g.,wherein at least one of R_(f), R_(g) and R_(h) are independentlyselected from aryl or heteroaryl, such as pyridinyl, pyridazinyl,pyrimidinyl, and pyrazinyl).

The term “carbonyl” as used herein refers to —C(O)—.

The term “carboxy” or “carboxylate” as used herein refers to R_(j)—COOHor its corresponding carboxylate salts (e.g., R_(j)—COONa), where R_(j)can independently be selected from alkoxy, aryloxy, alkyl, alkenyl,alkynyl, amide, amino, aryl, arylalkyl, cycloalkyl, ether, haloalkyl,heteroaryl, and heterocyclyl. Exemplary carboxys include, but are notlimited to, alkyl carboxy wherein R_(j) is alkyl, such as —O—C(O)-alkyl.Exemplary carboxy also include aryl or heteoraryl carboxy, e.g. whereinR_(j) is an aryl, such as phenyl and tolyl, or heteroaryl group such aspyridine, pyridazine, pyrimidine and pyrazine. The term carboxy alsoincludes “carboxycarbonyl,” e.g. a carboxy group attached to a carbonylgroup, e.g., —C(O)—COOH or salts, such as —C(O)—COONa.

The term “dicarboxylic acid” as used herein refers to a group containingat least two carboxylic acid groups such as saturated and unsaturatedhydrocarbon dicarboxylic acids and salts thereof. Exemplary dicarboxylicacids include alkyl dicarboxylic acids. Dicarboxylic acids include, butare not limited to succinic acid, glutaric acid, adipic acid, subericacid, sebacic acid, azelaic acid, maleic acid, phthalic acid, asparticacid, glutamic acid, malonic acid, fumaric acid, (+)/(−)-malic acid,(+)/(−) tartaric acid, isophthalic acid, and terephthalic acid.Dicarboxylic acids further include carboxylic acid derivatives thereof,such as anhydrides, imides, hydrazides (for example, succinic anhydrideand succinimide).

The term “cyano” as used herein refers to —CN.

The term “ester” refers to the structure —C(O)O—, —C(O)O—R_(i)—,—R_(j)C(O)O—R_(i)—, or —R_(j)C(O)O—, where O is not bound to hydrogen,and R_(i) and R_(j) can independently be selected from alkoxy, aryloxy,alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl, cycloalkyl,ether, haloalkyl, heteroaryl, and heterocyclyl. R_(i) can be a hydrogen,but R_(j) cannot be hydrogen. The ester may be cyclic, for example thecarbon atom and R_(j), the oxygen atom and or R_(i), or R_(i) and R_(j)may be joined to form a 3- to 12-membered ring. Exemplary estersinclude, but are not limited to, alkyl esters wherein at least one ofR_(i) or R_(j) is alkyl, such as —O—C(O)-alkyl, —C(O)—O-alkyl-, and-alkyl-C(O)—O-alkyl-. Exemplary esters also include aryl or heteroarylesters, e.g. wherein at least one of R_(i) or R_(j) is an aryl group,such as phenyl or tolyl, or a heteroaryl group, such as pyridine,pyridazine, pyrimidine or pyrazine, such as a nicotinate ester.Exemplary esters also include reverse esters having the structure—R_(j)C(O)O—, where the oxygen is bound to the parent molecule.Exemplary reverse esters include succinate, D-argininate, L-argininate,L-lysinate and D-lysinate. Esters also include carboxylic acidanhydrides and acid halides.

The term “ether” refers to the structure —R_(k)O—R_(l)—, where R_(k) andR_(l) can independently be alkyl, alkenyl, alkynyl, aryl, cycloalkyl,heterocyclyl, and ether. The ether can be attached to the parentmolecular group through R_(k) or R_(l). Exemplary ethers include, butare not limited to, alkoxyalkyl and alkoxyaryl groups. Ethers alsoincludes polyethers, e.g., where one or both of R_(k) and R_(l) areethers.

The terms “halo” or “halogen” or “hal” or “halide” as used herein referto F, Cl, Br, or I.

The term “haloalkyl” as used herein refers to an alkyl group substitutedwith one or more halogen atoms. “Haloalkyls” also encompass alkenyl oralkynyl groups substituted with one or more halogen atoms.

The terms “hydroxy” and “hydroxyl” as used herein refers to —OH.

The term “hydroxyalkyl” as used herein refers to a hydroxy attached toan alkyl group.

The term “hydroxyaryl” as used herein refers to a hydroxy attached to anaryl group.

The term “ketone” as used herein refers to the structure —C(O)—R_(m)(such as acetyl, —C(O)CH₃) or —R_(m)—C(O)—R_(n)—. The ketone can beattached to another group through R_(m) or R_(n). R_(m) or R_(n) can bealkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl or aryl, or R_(m) orR_(n) can be joined to form, for example, a 3- to 12-membered ring.

The term “monoester” as used herein refers to an analogue of adicarboxylic acid wherein one of the carboxylic acids is functionalizedas an ester and the other carboxylic acid is a free carboxylic acid orsalt of a carboxylic acid. Examples of monoesters include, but are notlimited to, to monoesters of succinic acid, glutaric acid, adipic acid,suberic acid, sebacic acid, azelaic acid, oxalic and maleic acid.

The term “nitro” as used herein refers to —NO₂.

The term “nitrate” as used herein refers to NO₃ ⁻.

The term “perfluoroalkyl” as used herein refers to an alkyl group inwhich all of the hydrogen atoms have been replaced by fluorine atoms.Exemplary perfluoroalkyl groups include, but are not limited to, C₁-C₅perfluoroalkyl, such as trifluoromethyl.

The term “perfluorocycloalkyl” as used herein refers to a cycloalkylgroup in which all of the hydrogen atoms have been replaced by fluorineatoms.

The term “perfluoroalkoxy” as used herein refers to an alkoxy group inwhich all of the hydrogen atoms have been replaced by fluorine atoms.

The term “phosphate” as used herein refers to the structure —OP(O)O₂ ²⁻,—R_(o)OP(O)O₂ ²⁻, —OP(O)(OR_(q))O⁻, or —R_(o)OP(O)(OR_(p))O⁻, whereinR_(o), R_(p) and R_(q) each independently can be alkyl, alkenyl,alkynyl, aryl, cycloalkyl, heterocyclyl, or hydrogen.

The term “sulfide” as used herein refers to the structure —R_(q)S—,where R_(q) can be alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,haloalkyl, heteroaryl, heterocyclyl. The sulfide may be cyclic, forexample, forming a 3 to 12-membered ring. The term “alkylsulfide” asused herein refers to an alkyl group attached to a sulfur atom.

The term “sulfinyl” as used herein refers to the structure —S(O)O—,—R_(r)S(O)O—, —R_(r)S(O)OR_(s)—, or —S(O)OR_(s)—, wherein R_(r) andR_(s) can be alkyl, alkenyl, aryl, arylalkyl, cycloalkyl, haloalkyl,heteroaryl, heterocyclyl, hydroxyl. Exemplary sulfinyl groups include,but are not limited to, alkylsulfinyls wherein at least one of R_(r) orR_(s) is alkyl, alkenyl, or alkynyl.

The term “sulfonamide” as used herein refers to the structure—(R_(t))—N—S(O)₂—R_(v)— or —R_(t)(R_(u))N—S(O)₂—R_(v), where R_(t),R_(u), and R_(v) can be, for example, hydrogen, alkyl, alkenyl, alkynyl,aryl, cycloalkyl, and heterocyclyl. Exemplary sulfonamides includealkylsulfonamides (e.g., where R_(v) is alkyl), acylsulfonamides (e.g.,where R_(v) is aryl), cycloalkyl sulfonamides (e.g., where R_(v) iscycloalkyl), and heterocyclyl sulfonamides (e.g., where R_(v) isheterocyclyl).

The term “sulfonate” as used herein refers to a salt or ester of asulfonic acid. The term “sulfonic acid” refers to R_(w)SO₃H, where R_(w)is alkyl, alkenyl, alkynyl, aryl, cycloalkyl, or heterocyclyl (e.g.,alkylsulfonyl). The term “sulfonyl” as used herein refers to thestructure R_(x)SO₂—, where R_(x) can be alkyl, alkenyl, alkynyl, aryl,cycloalkyl, and heterocyclyl (e.g., alkylsulfonyl). The term“alkylsulfonyl” as used herein refers to an alkyl group attached to asulfonyl group. “Alkylsulfonyl” groups can optionally contain alkenyl oralkynyl groups.

The term “sulfonate” as used herein refers R_(w)SO₃ ⁻, where R_(w) isalkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocyclyl, hydroxyl,alkoxy, aroxy, or aralkoxy, where each of the alkyl, alkenyl, alkynyl,cycloalkyl, aryl, heteroaryl, alkoxy, aroxy, or aralkoxy optionally issubstituted. Non-limiting examples include triflate (also known astrifluoromethanesulfonate, CF₃SO₃ ⁻), benzenesulfonate, tosylate (alsoknown as toluenesulfonate), and the like.

The term “thioketone” refers to the structure —R_(y)—C(S)—R_(z)—. Theketone can be attached to another group through R_(y) or R_(z). R_(y) orR_(z) can be alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl or aryl,or R_(y) or R_(z) can be joined to form a ring, for example, a 3- to12-membered ring.

Each of the above groups may be optionally substituted. As used herein,the term “substituted” is contemplated to include all permissiblesubstituents of organic compounds, “permissible” being in the context ofthe chemical rules of valence known to those of ordinary skill in theart. It will be understood that “substituted” also includes that thesubstitution results in a stable compound, e.g., which does notspontaneously undergo transformation such as by rearrangement,cyclization, elimination, etc. In some cases, “substituted” maygenerally refer to replacement of a hydrogen with a substituent asdescribed herein. However, “substituted,” as used herein, does notencompass replacement and/or alteration of a functional group by which amolecule is identified, e.g., such that the “substituted” functionalgroup becomes, through substitution, a different functional group. Forexample, a “substituted phenyl group” must still comprise the phenylmoiety and cannot be modified by substitution, in this definition, tobecome, e.g., a pyridine ring.

In a broad aspect, the permissible substituents include acyclic andcyclic, branched and unbranched, carbocyclic and heterocyclic, aromaticand nonaromatic substituents of organic compounds. Illustrativesubstituents include, for example, those described herein. Thepermissible substituents can be one or more and the same or differentfor appropriate organic compounds. For purposes of the presentteachings, the heteroatoms such as nitrogen may have hydrogensubstituents and/or any permissible substituents of organic compoundsdescribed herein which satisfy the valencies of the heteroatoms.

In various embodiments, the substituent is selected from alkoxy,aryloxy, alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl,carbamate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen,haloalkyl, heteroaryl, heterocyclyl, hydroxyl, ketone, nitro, phosphate,sulfide, sulfinyl, sulfonyl, sulfonic acid, sulfonamide, and thioketone,each of which optionally is substituted with one or more suitablesubstituents. In some embodiments, the substituent is selected fromalkoxy, aryloxy, alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl,carbamate, carboxy, cycloalkyl, ester, ether, formyl, haloalkyl,heteroaryl, heterocyclyl, ketone, phosphate, sulfide, sulfinyl,sulfonyl, sulfonic acid, sulfonamide, and thioketone, wherein each ofthe alkoxy, aryloxy, alkyl, alkenyl, alkynyl, amide, amino, aryl,arylalkyl, carbamate, carboxy, cycloalkyl, ester, ether, formyl,haloalkyl, heteroaryl, heterocyclyl, ketone, phosphate, sulfide,sulfinyl, sulfonyl, sulfonic acid, sulfonamide, and thioketone can befurther substituted with one or more suitable substituents.

Examples of substituents include, but are not limited to, halogen,azide, alkyl, aralkyl, alkenyl, alkynyl, cycloalkyl, hydroxyl, alkoxyl,amino, nitro, sulfhydryl, imino, amido, phosphonate, phosphinate,carbonyl, carboxyl, silyl, ether, alkylthio, sulfonyl, sulfonamido,ketone, aldehyde, thioketone, ester, heterocyclyl, —CN, aryl, aryloxy,perhaloalkoxy, aralkoxy, heteroaryl, heteroaryloxy, heteroarylalkyl,heteroaralkoxy, azido, alkylthio, oxo, acylalkyl, carboxy esters,carboxamido, acyloxy, aminoalkyl, alkylaminoaryl, alkylaryl,alkylaminoalkyl, alkoxyaryl, acylamino, aralkylamino, alkylsulfonyl,carboxamidoalkylaryl, carboxamidoaryl, hydroxyalkyl, haloalkyl,alkylaminoalkylcarboxy, aminocarboxamidoalkyl, cyano, alkoxyalkyl,perhaloalkyl, arylalkyloxyalkyl, and the like. In some embodiments, thesubstituent is selected from cyano, halogen, hydroxyl, and nitro.

As a non-limiting example, in various embodiments when one of the R_(a),R_(b), and R_(b′) in NR_(a)R_(b)R_(b′), referred to herein as an amineor amino, is selected from alkyl, alkenyl, alkynyl, cycloalkyl, andheterocyclyl, each of the alkyl, alkenyl, alkynyl, cycloalkyl, andheterocyclyl independently can be optionally substituted with one ormore substituents each independently selected from alkoxy, aryloxy,alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl, carbamate,carboxy, cycloalkyl, ester, ether, formyl, haloalkyl, heteroaryl,heterocyclyl, ketone, phosphate, sulfide, sulfinyl, sulfonyl, sulfonicacid, sulfonamide, and thioketone, wherein each of the alkoxy, aryloxy,alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl, carbamate,carboxy, cycloalkyl, ester, ether, formyl, haloalkyl, heteroaryl,heterocyclyl, ketone, phosphate, sulfide, sulfinyl, sulfonyl, sulfonicacid, sulfonamide, and thioketone can be further substituted with one ormore suitable substituents. In some embodiments when the amine is analkyl amine or a cycloalkylamine, the alkyl or the cycloalkyl can besubstituted with one or more substituents each independently selectedfrom alkoxy, aryloxy, alkyl, alkenyl, alkynyl, amide, amino, aryl,arylalkyl, carbamate, carboxy, cyano, cycloalkyl, ester, ether, formyl,halogen, haloalkyl, heteroaryl, heterocyclyl, hydroxyl, ketone, nitro,phosphate, sulfide, sulfinyl, sulfonyl, sulfonic acid, sulfonamide, andthioketone. In certain embodiments when the amine is an alkyl amine or acycloalkylamine, the alkyl or the cycloalkyl can be substituted with oneor more substituents each independently selected from amino, carboxy,cyano, and hydroxyl. For example, the alkyl or the cycloalkyl in thealkyl amine or the cycloalkylamine is substituted with an amino group,forming a diamine.

As used herein, a “suitable substituent” refers to a group that does notnullify the synthetic or pharmaceutical utility of the compounds of theinvention or the intermediates useful for preparing them. Examples ofsuitable substituents include, but are not limited to: (C₁-C₂₂),(C₁-C₈), (C₁-C₆), or (C₁-C₄) alkyl, alkenyl or alkynyl; (C₆-C₂₂),(C₆-C₁₈), (C₆-C₁₄), or (C₆-C₁₀) aryl; (C₂-C₂₁), (C₂-C₁₇), (C₂-C₁₃), or(C₂-C₉) heteroaryl; (C₃-C₂₂), (C₃-C₁₂), or (C₃-C₈) cycloalkyl; (C₁-C₂₂),(C₁-C₈), (C₁-C₆), or (C₁-C₄) alkoxy; (C₆-C₂₂), (C₆-C₁₈), (C₆-C₁₄), or(C₆-C₁₀) aryloxy; —CN; —OH; oxo; halo; carboxy; amino, such as—NH((C₁-C₂₂), (C₁-C₈), (C₁-C₆), or (C₁-C₄) alkyl), —N((C₁-C₂₂), (C₁-C₈),(C₁-C₆), or (C₁-C₄) alkyl)₂, —NH((C₆)aryl), or —N((C₆-C₁₀)aryl)₂;formyl; ketones, such as —CO((C₁-C₂₂), (C₁-C₈), (C₁-C₆), or (C₁-C₄)alkyl), —CO(((C₆-C₁₀) aryl) esters, such as —CO₂((C₁-C₂₂), (C₁-C₈),(C₁-C₆), or (C₁-C₄) alkyl) and —CO₂((C₆-C₁₀) aryl). One of skill in artcan readily choose a suitable substituent based on the stability andpharmacological and synthetic activity of the compound of the invention.

The term “pharmaceutically acceptable counter ion” refers to apharmaceutically acceptable anion or cation. In various embodiments, thepharmaceutically acceptable counter ion is a pharmaceutically acceptableion. For example, the pharmaceutically acceptable counter ion isselected from citrate, malate, acetate, oxalate, chloride, bromide,iodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate,isonicotinate, acetate, lactate, salicylate, tartrate, oleate, tannate,pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate,fumarate, gluconate, glucaronate, saccharate, formate, benzoate,glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate,p-toluenesulfonate and pamoate (i.e.,1,1′-methylene-bis-(2-hydroxy-3-naphthoate)). In some embodiments, thepharmaceutically acceptable counter ion is selected from chloride,bromide, iodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate,citrate, malate, acetate, oxalate, acetate, and lactate. In particularembodiments, the pharmaceutically acceptable counter ion is selectedfrom chloride, bromide, iodide, nitrate, sulfate, bisulfate, andphosphate.

The term “pharmaceutically acceptable salt(s)” refers to salts of acidicor basic groups that may be present in compounds used in the presentteachings. Compounds included in the present teachings that are basic innature are capable of forming a wide variety of salts with variousinorganic and organic acids. The acids that may be used to preparepharmaceutically acceptable acid addition salts of such basic compoundsare those that form non-toxic acid addition salts, i.e., saltscontaining pharmacologically acceptable anions, including but notlimited to sulfate, citrate, malate, acetate, oxalate, chloride,bromide, iodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate,isonicotinate, acetate, lactate, salicylate, citrate, tartrate, oleate,tannate, pantothenate, bitart rate, ascorbate, succinate, maleate,gentisinate, fumarate, gluconate, glucaronate, saccharate, formate,benzoate, glutamate, methanesulfonate, ethanesulfonate,benzenesulfonate, p-toluenesulfonate and pamoate (i.e.,1,1′-methylene-bis-(2-hydroxy-3-naphthoate)) salts. Compounds includedin the present teachings that include an amino moiety may formpharmaceutically acceptable salts with various amino acids, in additionto the acids mentioned above. Compounds included in the presentteachings, that are acidic in nature are capable of forming base saltswith various pharmacologically acceptable cations. Examples of suchsalts include alkali metal or alkaline earth metal salts and,particularly, calcium, magnesium, sodium, lithium, zinc, potassium, andiron salts.

In addition, if the compounds described herein are obtained as an acidaddition salt, the free base can be obtained by basifying a solution ofthe acid salt. Conversely, if the product is a free base, an additionsalt, particularly a pharmaceutically acceptable addition salt, may beproduced by dissolving the free base in a suitable organic solvent andtreating the solution with an acid, in accordance with conventionalprocedures for preparing acid addition salts from base compounds. Thoseskilled in the art will recognize various synthetic methodologies thatmay be used to prepare non-toxic pharmaceutically acceptable additionsalts.

A pharmaceutically acceptable salt can be derived from an acid selectedfrom 1-hydroxy-2-naphthoic acid, 2,2-dichloroacetic acid,2-hydroxyethanesulfonic acid, 2-oxoglutaric acid, 4-acetamidobenzoicacid, 4-aminosalicylic acid, acetic acid, adipic acid, ascorbic acid,aspartic acid, benzenesulfonic acid, benzoic acid, camphoric acid,camphor-10-sulfonic acid, capric acid (decanoic acid), caproic acid(hexanoic acid), caprylic acid (octanoic acid), carbonic acid, cinnamicacid, citric acid, cyclamic acid, dodecylsulfuric acid,ethane-1,2-disulfonic acid, ethanesulfonic acid, formic acid, fumaricacid, galactaric acid, gentisic acid, glucoheptonic acid, gluconic acid,glucuronic acid, glutamic acid, glutaric acid, glycerophosphoric acid,glycolic acid, hippuric acid, hydrobromic acid, hydrochloric acid,isethionic, isobutyric acid, lactic acid, lactobionic acid, lauric acid,maleic acid, malic acid, malonic acid, mandelic acid, methanesulfonicacid, mucic, naphthalene-1,5-disulfonic acid, naphthalene-2-sulfonicacid, nicotinic acid, nitric acid, oleic acid, oxalic acid, palmiticacid, pamoic acid, pantothenic, phosphoric acid, proprionic acid,pyroglutamic acid, salicylic acid, sebacic acid, stearic acid, succinicacid, sulfuric acid, tartaric acid, thiocyanic acid, toluenesulfonicacid, trifluoroacetic, and undecylenic acid.

Unless otherwise specified, the chemical groups include theircorresponding monovalent, divalent, trivalent, and tetravalent groups.For example, methyl includes monovalent methyl (—CH₃), divalent methyl(—CH₂—, methylyl), trivalent methyl

and tetravalent methyl

Unless otherwise specified, all numbers expressing quantities ofingredients, reaction conditions, and other properties or parametersused in the specification and claims are to be understood as beingmodified in all instances by the term “about.” Accordingly, unlessotherwise indicated, it should be understood that the numericalparameters set forth in the following specification and attached claimsare approximations. At the very least, and not as an attempt to limitthe application of the doctrine of equivalents to the scope of theclaims, numerical parameters should be read in light of the number ofreported significant digits and the application of ordinary roundingtechniques. For example, the term “about” can encompass variations of±10%, ±5%, ±2%, ±1%, ±0.5%, or ±0.1% of the numerical value of thenumber which the term “about” modifies. In various embodiments, the term“about” encompasses variations of ±5%, ±2%, ±1%, or ±0.5% of thenumerical value of the number. In some embodiments, the term “about”encompasses variations of ±5%, ±2%, or ±1% of the numerical value of thenumber. In certain embodiments, the term “about” encompasses variationsof ±5% of the numerical value of the number. In certain embodiments, theterm “about” encompasses variations of ±2% of the numerical value of thenumber. In certain embodiments, the term “about” encompasses variationsof ±1% of the numerical value of the number.

All numerical ranges herein include all numerical values and ranges ofall numerical values within the recited range of numerical values. As anon-limiting example, (C₁-C₆) alkyls also include any one of C₁, C₂, C₃,C₄, C₅, C₆, (C₁-C₂), (C₁-C₃), (C₁-C₄), (C₁-C₅), (C₂-C₃), (C₂-C₄),(C₂-C₅), (C₂-C₆), (C₃-C₄), (C₃-C₅), (C₃-C₆), (C₄-C₅), (C₄-C₆), and(C₅-C₆) alkyls.

Further, while the numerical ranges and parameters setting forth thebroad scope of the disclosure are approximations as discussed above, thenumerical values set forth in the Examples section are reported asprecisely as possible. It should be understood, however, that suchnumerical values inherently contain certain errors resulting from themeasurement equipment and/or measurement technique.

The present teachings generally provide Pt(IV)M compounds and/or Pt(IV)Mconjugates, compositions, and methods of using the compounds, conjugatesor compositions.

Compounds

In various embodiments provided herein, a platinum (IV) (Pt(IV))compound includes a suitable reacting group for reacting with afunctional group on a protein, engineered protein, antibody, antibodyfragment, peptide, agonist, antagonist, aptamer or ligand which may becapable of recognizing a selected target cell population, and/orderivatives/analogs/mimics thereof. The reacting group possessesprotein-conjugating properties, i.e., it binds covalently to theprotein. For example, the reacting group can be introduced by a linkerbetween the reacting group and platinum. In various embodiments, one ofor both the axial positions of platinum each comprises one or morereacting groups.

In some embodiments, the protein is albumin and/orderivatives/analogs/mimics thereof.

In some embodiments, the reacting group is a Michael acceptor such asmaleimide.

In some embodiments, a compound of the present teachings has Formula I:

or a pharmaceutically acceptable salt thereof, wherein:X and Y are independently selected from NH, alkyl and aryl;R¹ and R² each is Cl, or R¹ and R² are joined to form an oxalate;R³ is hydrogen, alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl,wherein each of the alkyl, alkenyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl groups optionally is substituted with one or more groups,each independently selected from halogen, cyano, nitro, hydroxyl,carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl, wherein each of the carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, or heterocyclyl is optionallysubstituted with one or more groups, each independently selected fromhalogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, heterocyclyl;R⁴ and R⁵ are each H or together constitute a cyclohexyl ring;Z is alternatively absent or alkyl, aryl, cycloalkyl, heterocyclyl,aryl, and heteroaryl, wherein each of the alkyl, alkenyl, cycloalkyl,heterocyclyl, aryl, and heteroaryl groups optionally is substituted withone or more groups, each independently selected from halogen, cyano,nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino,amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl, or alkylidene hydrazine wherein each of thecarboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl or alkylidene hydrazine is optionally substituted with oneor more groups, each independently selected from halogen, cyano, nitro,hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide,carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl; andR⁶ is a suitable reacting group for reacting with amino groups, hydroxylgroups or thiol groups, forming a conjugate with a protein, engineeredprotein, antibody, antibody fragment, peptide, agonist, antagonist,aptamer or ligand which may be capable of recognizing a selected targetcell population, and/or derivatives/analogs/mimics thereof, and whereinR⁶ is selected from any of the following groups:

where R⁷ is Cl, Br, F, mesylate, tosylate, O-(4-nitrophenyl),O-pentafluorophenyl. The reacting group can also be an activateddisulfide group, a vinylcarbonyl group, a vinyl acetylene group, anepoxide, an aziridine group or an acetylene group. The groups may besubstituted, where appropriate.

An embodiment of the invention is a compound or a pharmaceuticallyacceptable salt thereof wherein X together with R³ is selected from thegroup consisting of:

In some embodiments, the reacting group may comprise a maleimide. Suchcompounds may be referred to herein as “monomaleimide compounds”, i.e.,Pt(IV)M monomaleimide compounds. As used herein, “monomaleimidecompounds” are compounds with a single maleimide group. Themonomaleimide compound has Formula II:

or a pharmaceutically acceptable salt thereof, wherein:X and Y are independently selected from NH, alkyl and aryl;R¹ and R² each is Cl, or R¹ and R² are joined to form an oxalate;R³ is hydrogen, alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl,wherein each of the alkyl, alkenyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl groups optionally is substituted with one or more groups,each independently selected from halogen, cyano, nitro, hydroxyl,carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl, wherein each of the carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, or heterocyclyl is optionallysubstituted with one or more groups, each independently selected fromhalogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, heterocyclyl;R⁴ and R⁵ are each H or together constitute a cyclohexyl ring; andZ is alternatively absent or alkyl, aryl, cycloalkyl, heterocyclyl,aryl, and heteroaryl, wherein each of the alkyl, alkenyl, cycloalkyl,heterocyclyl, aryl, and heteroaryl groups optionally is substituted withone or more groups, each independently selected from halogen, cyano,nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino,amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl, or alkylidene hydrazine wherein each of thecarboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl or alkylidene hydrazine is optionally substituted with oneor more groups, each independently selected from halogen, cyano, nitro,hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide,carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl.

Not willing to be bound to any theory, the unsymmetrical nature ofPt(IV)M monomaleimide compounds allows for the modulation of platinumdrug release.

Another embodiment of the invention is a maleimide compound or apharmaceutically acceptable salt thereof wherein Y together with Z andthe maleimide is selected from the group consisting of:

Another embodiment of the invention is a maleimide compound havingFormula IIa:

or a pharmaceutically acceptable salt thereof, wherein:X and Y are independently selected from NH, alkyl and aryl;R¹ and R² each is Cl, or R¹ and R² are joined to form an oxalate;R³ is hydrogen, alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl,wherein each of the alkyl, alkenyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl groups optionally is substituted with one or more groups,each independently selected from halogen, cyano, nitro, hydroxyl,carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl, wherein each of the carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, or heterocyclyl is optionallysubstituted with one or more groups, each independently selected fromhalogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, heterocyclyl; andZ is alternatively absent or alkyl, aryl, cycloalkyl, heterocyclyl,aryl, and heteroaryl, wherein each of the alkyl, alkenyl, cycloalkyl,heterocyclyl, aryl, and heteroaryl groups optionally is substituted withone or more groups, each independently selected from halogen, cyano,nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino,amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl, or alkylidene hydrazine wherein each of thecarboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl or alkylidene hydrazine is optionally substituted with oneor more groups, each independently selected from halogen, cyano, nitro,hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide,carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl.

Another embodiment of the invention is a maleimide compounds havingFormula IIb:

or a pharmaceutically acceptable salt thereof, wherein:X and Y are independently selected from NH, alkyl and aryl;R¹ and R² each is Cl, or R¹ and R² are joined to form an oxalate;R³ is hydrogen, alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl,wherein each of the alkyl, alkenyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl groups optionally is substituted with one or more groups,each independently selected from halogen, cyano, nitro, hydroxyl,carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl, wherein each of the carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, or heterocyclyl is optionallysubstituted with one or more groups, each independently selected fromhalogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, heterocyclyl; andZ is alternatively absent or alkyl, aryl, cycloalkyl, heterocyclyl,aryl, and heteroaryl, wherein each of the alkyl, alkenyl, cycloalkyl,heterocyclyl, aryl, and heteroaryl groups optionally is substituted withone or more groups, each independently selected from halogen, cyano,nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino,amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl, or alkylidene hydrazine wherein each of thecarboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate,alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl,heterocyclyl or alkylidene hydrazine is optionally substituted with oneor more groups, each independently selected from halogen, cyano, nitro,hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide,carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl.

A non-limiting example of a Pt(IV)M compound of the invention is acompound selected from the group consisting of the compounds listed:

Another non-limiting example of a Pt(IV)M compound of the invention is acompound selected from the group consisting of the compounds listed:

As described herein, some compounds of the present teachings may beprovided as a salt comprising a charged platinum complex and a counterion, including a pharmaceutically acceptable counter ion. The counterion may be a weak or non-nucleophilic stabilizing ion, having a chargeof (−1), (−2), (−3), (+1), (+2), (+3), etc. In some embodiments, thecounter ion has a charge of (−1). In other embodiments, the counter ionhas a charge of (−2). In some embodiments, the counter ion has a chargeof (+1). In other embodiments, the counter ion has a charge of (+2).

The present teachings further comprise compositions (includingpharmaceutical compositions) each comprising one or more of thecompounds as described herein, and at least one pharmaceuticallyacceptable excipient.

Formulation, Delivery, Administration, and Dosing

In some embodiments, compositions are administered to humans, humanpatients or subjects. For the purposes of the present disclosure, thephrase “active ingredient” generally refers to the Pt(IV)M compoundsand/or Pt(IV)M conjugates to be delivered as described herein.

Although the descriptions of pharmaceutical compositions provided hereinare principally directed to pharmaceutical compositions which aresuitable for administration to humans, it will be understood by theskilled artisan that such compositions are generally suitable foradministration to any other animal, e.g., to non-human animals, e.g.non-human mammals. Modification of pharmaceutical compositions suitablefor administration to humans in order to render the compositionssuitable for administration to various animals is well understood, andthe ordinarily skilled veterinary pharmacologist can design and/orperform such modification with merely ordinary, if any, experimentation.Subjects to which administration of the pharmaceutical compositions iscontemplated include, but are not limited to, humans and/or otherprimates; mammals, including commercially relevant mammals such ascattle, pigs, horses, sheep, cats, dogs, mice, and/or rats; and/orbirds, including commercially relevant birds such as poultry, chickens,ducks, geese, and/or turkeys.

Formulations of the pharmaceutical compositions described herein may beprepared by any method known or hereafter developed in the art ofpharmacology. In general, such preparatory methods include the step ofbringing the active ingredient into association with an excipient and/orone or more other accessory ingredients, and then, if necessary and/ordesirable, dividing, shaping and/or packaging the product into a desiredsingle- or multi-dose unit.

A pharmaceutical composition in accordance with the invention may beprepared, packaged, and/or sold in bulk, as a single unit dose, and/oras a plurality of single unit doses. As used herein, a “unit dose” isdiscrete amount of the pharmaceutical composition comprising apredetermined amount of the active ingredient. The amount of the activeingredient is generally equal to the dosage of the active ingredientwhich would be administered to a subject and/or a convenient fraction ofsuch a dosage such as, for example, one-half or one-third of such adosage.

Relative amounts of the active ingredient, the pharmaceuticallyacceptable excipient, and/or any additional ingredients in apharmaceutical composition in accordance with the invention will vary,depending upon the identity, size, and/or condition of the subjecttreated and further depending upon the route by which the composition isto be administered. By way of example, the composition may comprisebetween 0.1% and 100%, e.g., between 0.5 and 50%, between 1-30%, between5-80%, at least 80% (w/w) active ingredient.

The Pt(IV)M compounds and/or Pt(IV)M conjugates of the present inventioncan be formulated using one or more excipients to: (1) increasestability; (2) permit the sustained or delayed release (e.g., from adepot formulation of the Pt(IV)M compounds and/or Pt(IV)M conjugates);(3) alter the biodistribution (e.g., target the Pt(IV)M compounds and/orPt(IV)M conjugates to specific tissues or cell types); (4) alter therelease profile of the Pt(IV)M compounds and/or Pt(IV)M conjugates invivo. Non-limiting examples of the excipients include any and allsolvents, dispersion media, diluents, or other liquid vehicles,dispersion or suspension aids, surface active agents, isotonic agents,thickening or emulsifying agents, and preservatives. Excipients of thepresent invention may also include, without limitation, lipidoids,liposomes, lipid nanoparticles, polymers, lipoplexes, core-shellnanoparticles, peptides, proteins, hyaluronidase, nanoparticle mimicsand combinations thereof. Accordingly, the formulations of the inventionmay include one or more excipients, each in an amount that togetherincreases the stability of the Pt(IV)M compounds and/or Pt(IV)Mconjugates.

In some embodiments, the pH value of the pharmaceutical composition isbetween about 4 to about 7, between 4 and 6, between 4 and 5, about 4,about 5, about 6 or about 7.

Excipients

Pharmaceutical formulations may additionally comprise a pharmaceuticallyacceptable excipient, which, as used herein, includes any and allsolvents, dispersion media, diluents, or other liquid vehicles,dispersion or suspension aids, surface active agents, isotonic agents,thickening or emulsifying agents, preservatives, solid binders,lubricants and the like, as suited to the particular dosage formdesired. Remington's The Science and Practice of Pharmacy, 21st Edition,A. R. Gennaro (Lippincott, Williams & Wilkins, Baltimore, Md., 2006;incorporated herein by reference in its entirety) discloses variousexcipients used in formulating pharmaceutical compositions and knowntechniques for the preparation thereof. Except insofar as anyconventional excipient medium is incompatible with a substance or itsderivatives, such as by producing any undesirable biological effect orotherwise interacting in a deleterious manner with any othercomponent(s) of the pharmaceutical composition, its use is contemplatedto be within the scope of this invention.

In some embodiments, a pharmaceutically acceptable excipient is at least95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100%pure. In some embodiments, an excipient is approved for use in humansand for veterinary use. In some embodiments, an excipient is approved byUnited States Food and Drug Administration. In some embodiments, anexcipient is pharmaceutical grade. In some embodiments, an excipientmeets the standards of the United States Pharmacopoeia (USP), theEuropean Pharmacopoeia (EP), the British Pharmacopoeia, and/or theInternational Pharmacopoeia.

Pharmaceutically acceptable excipients used in the manufacture ofpharmaceutical compositions include, but are not limited to, inertdiluents, dispersing and/or granulating agents, surface active agentsand/or emulsifiers, disintegrating agents, binding agents,preservatives, buffering agents, lubricating agents, and/or oils. Suchexcipients may optionally be included in pharmaceutical compositions.

Exemplary diluents include, but are not limited to, calcium carbonate,sodium carbonate, calcium phosphate, dicalcium phosphate, calciumsulfate, calcium hydrogen phosphate, sodium phosphate lactose, sucrose,cellulose, microcrystalline cellulose, kaolin, mannitol, sorbitol,inositol, sodium chloride, dry starch, cornstarch, powdered sugar, etc.,and/or combinations thereof.

Exemplary granulating and/or dispersing agents include, but are notlimited to, potato starch, corn starch, tapioca starch, sodium starchglycolate, clays, alginic acid, guar gum, citrus pulp, agar, bentonite,cellulose and wood products, natural sponge, cation-exchange resins,calcium carbonate, silicates, sodium carbonate, cross-linkedpoly(vinyl-pyrrolidone) (crospovidone), sodium carboxymethyl starch(sodium starch glycolate), carboxymethyl cellulose, cross-linked sodiumcarboxymethyl cellulose (croscarmellose), methylcellulose,pregelatinized starch (starch 1500), microcrystalline starch, waterinsoluble starch, calcium carboxymethyl cellulose, magnesium aluminumsilicate (VEEGUM®), sodium lauryl sulfate, quaternary ammoniumcompounds, etc., and/or combinations thereof.

Exemplary surface active agents and/or emulsifiers include, but are notlimited to, natural emulsifiers (e.g. acacia, agar, alginic acid, sodiumalginate, tragacanth, chondrux, cholesterol, xanthan, pectin, gelatin,egg yolk, casein, wool fat, cholesterol, wax, and lecithin), colloidalclays (e.g. bentonite [aluminum silicate] and VEEGUM® [magnesiumaluminum silicate]), long chain amino acid derivatives, high molecularweight alcohols (e.g. stearyl alcohol, cetyl alcohol, oleyl alcohol,triacetin monostearate, ethylene glycol distearate, glycerylmonostearate, and propylene glycol monostearate, polyvinyl alcohol),carbomers (e.g. carboxy polymethylene, polyacrylic acid, acrylic acidpolymer, and carboxyvinyl polymer), carrageenan, cellulosic derivatives(e.g. carboxymethylcellulose sodium, powdered cellulose, hydroxymethylcellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose,methylcellulose), sorbitan fatty acid esters (e.g. polyoxyethylenesorbitan monolaurate [TWEEN®20], polyoxyethylene sorbitan [TWEENn®60],polyoxyethylene sorbitan monooleate [TWEEN®80], sorbitan monopalmitate[SPAN®40], sorbitan monostearate [SPAN®60], sorbitan tristearate[SPAN®65], glyceryl monooleate, sorbitan monooleate [SPAN®80]),polyoxyethylene esters (e.g. polyoxyethylene monostearate [MYRJ®45],polyoxyethylene hydrogenated castor oil, polyethoxylated castor oil,polyoxymethylene stearate, and SOLUTOL®), sucrose fatty acid esters,polyethylene glycol fatty acid esters (e.g. CREMOPHOR®), polyoxyethyleneethers, (e.g. polyoxyethylene lauryl ether [BRIJ®30]),poly(vinyl-pyrrolidone), diethylene glycol monolaurate, triethanolamineoleate, sodium oleate, potassium oleate, ethyl oleate, oleic acid, ethyllaurate, sodium lauryl sulfate, PLURONIC®F 68, POLOXAMER®188,cetrimonium bromide, cetylpyridinium chloride, benzalkonium chloride,docusate sodium, etc. and/or combinations thereof.

Exemplary binding agents include, but are not limited to, starch (e.g.cornstarch and starch paste); gelatin; sugars (e.g. sucrose, glucose,dextrose, dextrin, molasses, lactose, lactitol, mannitol); natural andsynthetic gums (e.g. acacia, sodium alginate, extract of Irish moss,panwar gum, ghatti gum, mucilage of isapol husks,carboxymethylcellulose, methylcellulose, ethylcellulose,hydroxyethylcellulose, hydroxypropyl cellulose, hydroxypropylmethylcellulose, microcrystalline cellulose, cellulose acetate,poly(vinyl-pyrrolidone), magnesium aluminum silicate (Veegum®), andlarch arabogalactan); alginates; polyethylene oxide; polyethyleneglycol; inorganic calcium salts; silicic acid; polymethacrylates; waxes;water; alcohol; etc.; and combinations thereof.

Exemplary preservatives may include, but are not limited to,antioxidants, chelating agents, antimicrobial preservatives, antifungalpreservatives, alcohol preservatives, acidic preservatives, and/or otherpreservatives. Exemplary antioxidants include, but are not limited to,alpha tocopherol, ascorbic acid, acorbyl palmitate, butylatedhydroxyanisole, butylated hydroxytoluene, monothioglycerol, potassiummetabisulfite, propionic acid, propyl gallate, sodium ascorbate, sodiumbisulfite, sodium metabisulfite, and/or sodium sulfite. Exemplarychelating agents include ethylenediaminetetraacetic acid (EDTA), citricacid monohydrate, disodium edetate, dipotassium edetate, edetic acid,fumaric acid, malic acid, phosphoric acid, sodium edetate, tartaricacid, and/or trisodium edetate. Exemplary antimicrobial preservativesinclude, but are not limited to, benzalkonium chloride, benzethoniumchloride, benzyl alcohol, bronopol, cetrimide, cetylpyridinium chloride,chlorhexidine, chlorobutanol, chlorocresol, chloroxylenol, cresol, ethylalcohol, glycerin, hexetidine, imidurea, phenol, phenoxyethanol,phenylethyl alcohol, phenylmercuric nitrate, propylene glycol, and/orthimerosal. Exemplary antifungal preservatives include, but are notlimited to, butyl paraben, methyl paraben, ethyl paraben, propylparaben, benzoic acid, hydroxybenzoic acid, potassium benzoate,potassium sorbate, sodium benzoate, sodium propionate, and/or sorbicacid. Exemplary alcohol preservatives include, but are not limited to,ethanol, polyethylene glycol, phenol, phenolic compounds, bisphenol,chlorobutanol, hydroxybenzoate, and/or phenylethyl alcohol. Exemplaryacidic preservatives include, but are not limited to, vitamin A, vitaminC, vitamin E, beta-carotene, citric acid, acetic acid, dehydroaceticacid, ascorbic acid, sorbic acid, and/or phytic acid. Otherpreservatives include, but are not limited to, tocopherol, tocopherolacetate, deteroxime mesylate, cetrimide, butylated hydroxyanisol (BHA),butylated hydroxytoluened (BHT), ethylenediamine, sodium lauryl sulfate(SLS), sodium lauryl ether sulfate (SLES), sodium bisulfite, sodiummetabisulfite, potassium sulfite, potassium metabisulfite, GLYDANTPLUS®, PHENONIP®, methylparaben, GERMALL® 115, GERMABEN® II, NEOLONE™,KATHON™, and/or EUXYL®.

Exemplary buffering agents include, but are not limited to, citratebuffer solutions, acetate buffer solutions, phosphate buffer solutions,ammonium chloride, calcium carbonate, calcium chloride, calcium citrate,calcium glubionate, calcium gluceptate, calcium gluconate, D-gluconicacid, calcium glycerophosphate, calcium lactate, propanoic acid, calciumlevulinate, pentanoic acid, dibasic calcium phosphate, phosphoric acid,tribasic calcium phosphate, calcium hydroxide phosphate, potassiumacetate, potassium chloride, potassium gluconate, potassium mixtures,dibasic potassium phosphate, monobasic potassium phosphate, potassiumphosphate mixtures, sodium acetate, sodium bicarbonate, sodium chloride,sodium citrate, sodium lactate, dibasic sodium phosphate, monobasicsodium phosphate, sodium phosphate mixtures, tromethamine, magnesiumhydroxide, aluminum hydroxide, alginic acid, pyrogen-free water,isotonic saline, Ringer's solution, ethyl alcohol, etc., and/orcombinations thereof.

Exemplary lubricating agents include, but are not limited to, magnesiumstearate, calcium stearate, stearic acid, silica, talc, malt, glycerylbehanate, hydrogenated vegetable oils, polyethylene glycol, sodiumbenzoate, sodium acetate, sodium chloride, leucine, magnesium laurylsulfate, sodium lauryl sulfate, etc., and combinations thereof.

Exemplary oils include, but are not limited to, almond, apricot kernel,avocado, babassu, bergamot, black current seed, borage, cade, camomile,canola, caraway, carnauba, castor, cinnamon, cocoa butter, coconut, codliver, coffee, corn, cotton seed, emu, eucalyptus, evening primrose,fish, flaxseed, geraniol, gourd, grape seed, hazel nut, hyssop,isopropyl myristate, jojoba, kukui nut, lavandin, lavender, lemon,litsea cubeba, macademia nut, mallow, mango seed, meadowfoam seed, mink,nutmeg, olive, orange, orange roughy, palm, palm kernel, peach kernel,peanut, poppy seed, pumpkin seed, rapeseed, rice bran, rosemary,safflower, sandalwood, sasquana, savoury, sea buckthorn, sesame, sheabutter, silicone, soybean, sunflower, tea tree, thistle, tsubaki,vetiver, walnut, and wheat germ oils. Exemplary oils include, but arenot limited to, butyl stearate, caprylic triglyceride, caprictriglyceride, cyclomethicone, diethyl sebacate, dimethicone 360,isopropyl myristate, mineral oil, octyldodecanol, oleyl alcohol,silicone oil, and/or combinations thereof.

Excipients such as cocoa butter and suppository waxes, coloring agents,coating agents, sweetening, flavoring, and/or perfuming agents can bepresent in the composition, according to the judgment of the formulator.

Administration

The Pt(IV)M compounds and/or Pt(IV)M conjugates of the present inventionmay be administered by any route which results in a therapeuticallyeffective outcome. These include, but are not limited to enteral,gastroenteral, epidural, oral, transdermal, epidural (peridural),intracerebral (into the cerebrum), intracerebroventricular (into thecerebral ventricles), epicutaneous (application onto the skin),intradermal, (into the skin itself), subcutaneous (under the skin),nasal administration (through the nose), intravenous (into a vein),intraarterial (into an artery), intramuscular (into a muscle),intracardiac (into the heart), intraosseous infusion (into the bonemarrow), intrathecal (into the spinal canal), intraperitoneal, (infusionor injection into the peritoneum), intravesical infusion, intravitreal,(through the eye), intracavernous injection, (into the base of thepenis), intravaginal administration, intrauterine, extra-amnioticadministration, transdermal (diffusion through the intact skin forsystemic distribution), transmucosal (diffusion through a mucousmembrane), insufflation (snorting), sublingual, sublabial, enema, eyedrops (onto the conjunctiva), or in ear drops. In specific embodiments,compositions may be administered in a way which allows them cross theblood-brain barrier, vascular barrier, or other epithelial barrier.

Dosing

The present invention provides methods comprising administering Pt(IV)Mcompounds and/or Pt(IV)M conjugates to a subject in need thereof.Pt(IV)M compounds as described herein may be administered to a subjectusing any amount and any route of administration effective forpreventing or treating or imaging a disease, disorder, and/or condition(e.g., a disease, disorder, and/or condition relating to working memorydeficits). The exact amount required will vary from subject to subject,depending on the species, age, and general condition of the subject, theseverity of the disease, the particular composition, its mode ofadministration, its mode of activity, and the like.

Compositions in accordance with the invention are typically formulatedin dosage unit form for ease of administration and uniformity of dosage.It will be understood, however, that the total daily usage of thecompositions of the present invention may be decided by the attendingphysician within the scope of sound medical judgment. The specifictherapeutically effective, prophylactically effective, or appropriateimaging dose level for any particular patient will depend upon a varietyof factors including the disorder being treated and the severity of thedisorder; the activity of the specific compound employed; the specificcomposition employed; the age, body weight, general health, sex and dietof the patient; the time of administration, route of administration, andrate of excretion of the specific compound employed; the duration of thetreatment; drugs used in combination or coincidental with the specificcompound employed; and like factors well known in the medical arts.

In some embodiments, compositions in accordance with the presentinvention may be administered at dosage levels sufficient to deliverfrom about 0.0001 mg/kg to about 100 mg/kg, from about 0.001 mg/kg toabout 0.05 mg/kg, from about 0.005 mg/kg to about 0.05 mg/kg, from about0.001 mg/kg to about 0.005 mg/kg, from about 0.05 mg/kg to about 0.5mg/kg, from about 0.01 mg/kg to about 50 mg/kg, from about 0.1 mg/kg toabout 40 mg/kg, from about 0.5 mg/kg to about 30 mg/kg, from about 0.01mg/kg to about 10 mg/kg, from about 0.1 mg/kg to about 10 mg/kg, or fromabout 1 mg/kg to about 25 mg/kg, of subject body weight per day, one ormore times a day, to obtain the desired therapeutic, diagnostic,prophylactic, or imaging effect. The desired dosage may be deliveredthree times a day, two times a day, once a day, every other day, everythird day, every week, every two weeks, every three weeks, or every fourweeks. In some embodiments, the desired dosage may be delivered usingmultiple administrations (e.g., two, three, four, five, six, seven,eight, nine, ten, eleven, twelve, thirteen, fourteen, or moreadministrations). When multiple administrations are employed, splitdosing regimens such as those described herein may be used.

As used herein, a “split dose” is the division of single unit dose ortotal daily dose into two or more doses, e.g, two or moreadministrations of the single unit dose. As used herein, a “single unitdose” is a dose of any therapeutic administered in one dose/at onetime/single route/single point of contact, i.e., single administrationevent. As used herein, a “total daily dose” is an amount given orprescribed in 24 hr period. It may be administered as a single unitdose. In one embodiment, the Pt(IV)M compounds and/or Pt(IV)M conjugatesof the present invention are administered to a subject in split doses.The Pt(IV)M compounds and/or Pt(IV)M conjugates may be formulated inbuffer only or in a formulation described herein.

Dosage Forms

A pharmaceutical composition described herein can be formulated into adosage form described herein, such as a topical, intranasal,intratracheal, or injectable (e.g., intravenous, intraocular,intravitreal, intramuscular, intracardiac, intraperitoneal,subcutaneous).

Liquid Dosage Forms

Liquid dosage forms for parenteral administration include, but are notlimited to, pharmaceutically acceptable emulsions, microemulsions,solutions, suspensions, syrups, and/or elixirs. In addition to activeingredients, liquid dosage forms may comprise inert diluents commonlyused in the art including, but not limited to, water or other solvents,solubilizing agents and emulsifiers such as ethyl alcohol, isopropylalcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzylbenzoate, propylene glycol, 1,3-butylene glycol, dimethylformamide, oils(in particular, cottonseed, groundnut, corn, germ, olive, castor, andsesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycolsand fatty acid esters of sorbitan, and mixtures thereof. In certainembodiments for parenteral administration, compositions may be mixedwith solubilizing agents such as CREMOPHOR®, alcohols, oils, modifiedoils, glycols, polysorbates, cyclodextrins, polymers, and/orcombinations thereof.

Injectable

Injectable preparations, for example, sterile injectable aqueous oroleaginous suspensions may be formulated according to the known art andmay include suitable dispersing agents, wetting agents, and/orsuspending agents. Sterile injectable preparations may be sterileinjectable solutions, suspensions, and/or emulsions in nontoxicparenterally acceptable diluents and/or solvents, for example, asolution in 1,3-butanediol. Among the acceptable vehicles and solventsthat may be employed include, but are not limited to, water, Ringer'ssolution, U.S.P., and isotonic sodium chloride solution. Sterile, fixedoils are conventionally employed as a solvent or suspending medium. Forthis purpose any bland fixed oil can be employed including syntheticmono- or diglycerides. Fatty acids such as oleic acid can be used in thepreparation of injectables.

Injectable formulations can be sterilized, for example, by filtrationthrough a bacterial-retaining filter, and/or by incorporatingsterilizing agents in the form of sterile solid compositions which canbe dissolved or dispersed in sterile water or other sterile injectablemedium prior to use.

In order to prolong the effect of an active ingredient, it may bedesirable to slow the absorption of the active ingredient fromsubcutaneous or intramuscular injection. This may be accomplished by theuse of a liquid suspension of crystalline or amorphous material withpoor water solubility. The rate of absorption of the Pt(IV)M compoundsand/or Pt(IV)M conjugates then depends upon its rate of dissolutionwhich, in turn, may depend upon crystal size and crystalline form.Alternatively, delayed absorption of a parenterally administered Pt(IV)Mcompound and/or Pt(IV)M conjugates may be accomplished by dissolving orsuspending the monomalimide in an oil vehicle. Injectable depot formsare made by forming microencapsule matrices of the Pt(IV)M compoundsand/or Pt(IV)M conjugates in biodegradable polymers such aspolylactide-polyglycolide. Depending upon the ratio of Pt(IV)M compoundsand/or Pt(IV)M conjugates to polymer and the nature of the particularpolymer employed, the rate of Pt(IV)M compound and/or Pt(IV)M conjugatesrelease can be controlled. Examples of other biodegradable polymersinclude, but are not limited to, poly(orthoesters) and poly(anhydrides).Depot injectable formulations may be prepared by entrapping the Pt(IV)Mcompounds and/or Pt(IV)M conjugates in liposomes or microemulsions whichare compatible with body tissues.

Pulmonary

Formulations described herein as being useful for pulmonary delivery mayalso be used for intranasal delivery of a pharmaceutical composition.Another formulation suitable for intranasal administration may be acoarse powder comprising the active ingredient and having an averageparticle from about 0.2 um to 500 um. Such a formulation may beadministered in the manner in which snuff is taken, i.e. by rapidinhalation through the nasal passage from a container of the powder heldclose to the nose.

Formulations suitable for nasal administration may, for example,comprise from about as little as 0.1% (w/w) and as much as 100% (w/w) ofactive ingredient, and may comprise one or more of the additionalingredients described herein. A pharmaceutical composition may beprepared, packaged, and/or sold in a formulation suitable for buccaladministration. Such formulations may, for example, be in the form oftablets and/or lozenges made using conventional methods, and may, forexample, contain about 0.1% to 20% (w/w) active ingredient, where thebalance may comprise an orally dissolvable and/or degradable compositionand, optionally, one or more of the additional ingredients describedherein. Alternately, formulations suitable for buccal administration maycomprise a powder and/or an aerosolized and/or atomized solution and/orsuspension comprising active ingredient. Such powdered, aerosolized,and/or aerosolized formulations, when dispersed, may have an averageparticle and/or droplet size in the range from about 0.1 nm to about 200nm, and may further comprise one or more of any additional ingredientsdescribed herein.

General considerations in the formulation and/or manufacture ofpharmaceutical agents may be found, for example, in Remington: TheScience and Practice of Pharmacy 21st ed., Lippincott Williams &Wilkins, 2005 (incorporated herein by reference in its entirety).

Coatings or Shells

Solid dosage forms of tablets, dragees, capsules, pills, and granulescan be prepared with coatings and shells such as enteric coatings andother coatings well known in the pharmaceutical formulating art. Theymay optionally comprise opacifying agents and can be of a compositionthat they release the active ingredient(s) only, or preferentially, in acertain part of the intestinal tract, optionally, in a delayed manner.Examples of embedding compositions which can be used include polymericsubstances and waxes. Solid compositions of a similar type may beemployed as fillers in soft and hard-filled gelatin capsules using suchexcipients as lactose or milk sugar as well as high molecular weightpolyethylene glycols and the like.

Pharmaceutical Compositions and Methods of Use

Embodiments of the present teachings also relate to treating ahyperproliferative disorder, cancer and/or a tumor according to any ofthe techniques and compositions and combinations of compositionsdescribed herein.

In various embodiments, methods for treating a subject having a cancerare provided, wherein the method comprises administering atherapeutically-effective amount of a Pt(IV)M compound and/or Pt(IV)Mconjugate, as described herein, to a subject having a cancer, suspectedof having cancer, or having a predisposition to a cancer. According tothe present invention, cancer embraces any disease or maladycharacterized by uncontrolled cell proliferation, e.g.,hyperproliferation. Cancers may be characterized by tumors, e.g., solidtumors or any neoplasm.

In some embodiments, the subject may be otherwise free of indicationsfor treatment with the Pt(IV)M compound and/or Pt(IV)M conjugate. Insome embodiments, methods include use of cancer cells, including but notlimited to mammalian cancer cells. In some instances, the mammaliancancer cells are human cancer cells.

In some embodiments, the Pt(IV)M compound and/or Pt(IV)M conjugate ofthe present teachings have been found to inhibit cancer and/or tumorgrowth. They may also reduce cell proliferation, invasiveness, and/ormetastasis, thereby rendering them useful for the treatment of a cancer.

In some embodiments, the Pt(IV)M compound and/or Pt(IV)M conjugate ofthe present teachings may be used to prevent the growth of a tumor orcancer, and/or to prevent the metastasis of a tumor or cancer. In someembodiments, compositions of the present teachings may be used to shrinkor destroy a cancer.

In some embodiments, a Pt(IV)M compound and/or Pt(IV)M conjugateprovided herein is useful for inhibiting proliferation of a cancer cell.In some embodiments a compound provided herein is useful for inhibitingcellular proliferation, e.g., inhibiting the rate of cellularproliferation, preventing cellular proliferation, and/or inducing celldeath. In general, a compound as described herein can inhibit cellularproliferation of a cancer cell or both inhibiting proliferation and/orinducing cell death of a cancer cell.

The cancers treatable by methods of the present teachings generallyoccur in mammals. Mammals include, for example, humans, non-humanprimates, dogs, cats, rats, mice, rabbits, ferrets, guinea pigs horses,pigs, sheep, goats, and cattle. In various embodiments, the cancer islung cancer, e.g., small cell lung cancer, non-small cell lung cancer,squamous cell lung cancer, breast cancer, non-BRCA-associated breastcancer, colorectal cancer, colon cancer, ovarian cancer, pancreaticcancer, bladder cancer, prostate cancer, cervical cancer, renal cancer,leukemia, central nervous system cancers, myeloma, melanoma,mesothelioma, stomach cancer, rectal cancer, cancer of the largeintestine, cancer of the small intestine, esophageal cancer, uterinecancer, head and neck cancer, endometrial cancer, eye cancer, thyroidcancer, testicular cancer, bile duct cancer, liver cancer, kidneycancer, pituitary cancer, lymphoma, brain cancer, glioma, glioblastomamultiforme, meningioma, medulloblastoma, astrocytoma, neuroblastoma,basal cell carcinoma of the skin, sarcoma, synovial sarcoma,rhabdomyosarcoma, leiomyosarcoma, chondrosarcoma, and fibrosarcoma. Insome embodiments, the cancer is lung cancer. In certain embodiments, thecancer is human lung carcinoma, ovarian cancer, pancreatic cancer orcolorectal cancer including mutant BRCA1 and/or mutant BRCA2 ornon-BRCA-associated forms of these cancers.

In some embodiments, the Pt(IV)M compound and/or Pt(IV)M conjugate ofthe present teachings may be administered to the cancer cells havingBRCA1 mutations, BRCA2 mutations, ERCC1 or ERCC2 mutations, mutations inthe fanconi anemia genes, MLH1, MSH2, PTEN, Mutations in genes that codefor proteins involved in DNA repair, mutations in genes that code forproteins involved in non-homologous DNA repair, mutations in genes thatcode for proteins involved in nucleotide excision repair, mutations ingenes that code for proteins involved in DNA mismatch repair, genetictests that identify tumors that have a defect in DNA repair, changes inthe expression of genes involved in DNA repair such as ERCC1 or ERCC2,and so on. The mutations may be germline or somatic.

In another aspect, the Pt(IV)M compound and/or Pt(IV)M conjugate of thepresent teachings may be administered to cells with increased albuminuptake, for example, but not limited to, cells with mutations thatincrease micropinocytosis, cells with mitogen activated kinase pathwaymutations, cells with KRAS mutations, cells with BRAF mutations, cellswith RAC mutations, cells with RAS overexpression, cells with RAC1activation, or cells with CDC42 activation.

In some embodiments, cells with increased albumin update may beidentified with imaging techniques. For example, a contrast agent isadministered to a patient and the level of accumulation of the contrastagent at a tumor site is measured with an imaging technique. The imagingtechnique may be ultrasound, X-ray, single-photon emissiontomography/computed tomography (SPECT/CT), positron emissiontomography/computed tomography (PET/CT), magnetic resonance imaging(MRI), computed tomography (CT), single-photon emission tomography(SPECT), fluorescence tomography, and fluorescence spectroscopy.

In yet another aspect, the Pt(IV)M compound and/or Pt(IV)M conjugate ofthe present teachings may be administered to tumors with a high level ofenhanced permeability and retention (EPR) effect. In some embodiments,tumors with a high level of enhanced permeability and retention effectmay be identified with imaging techniques. As a non-limited example,iron oxide nanoparticle magnetic resonance imaging may be administeredto a patient and EPR effects are measured.

In some embodiments, the Pt(IV)M compound and/or Pt(IV)M conjugate ofthe present teachings may be administered to a subject selected with themethod disclosed in WO2015017506, the contents of which are incorporatedherein by reference in their entirety, the method comprising:

(a) administering a contrast agent to the subject;

(b) measuring the level of accumulation of the contrast agent at atleast one intended site of treatment; and

(c) selecting the subject based on the level of the accumulation of thecontrast agent; wherein the intended site of treatment is a tumor.

Kits and Devices

The invention provides a variety of kits and devices for convenientlyand/or effectively carrying out methods of the present invention.Typically kits will comprise sufficient amounts and/or numbers ofcomponents to allow a user to perform multiple treatments of asubject(s) and/or to perform multiple experiments.

In one embodiment, the present invention provides kits for inhibitingtumor cell growth in vitro or in vivo, comprising a Pt(IV)M compoundand/or Pt(IV)M conjugate of the present invention or a combination ofPt(IV)M compounds and/or Pt(IV)M conjugates of the present invention,optionally in combination with any other active agents.

The kit may further comprise packaging and instructions and/or adelivery agent to form a formulation composition. The delivery agent maycomprise a saline, a buffered solution, or any delivery agent disclosedherein. The amount of each component may be varied to enable consistent,reproducible higher concentration saline or simple buffer formulations.The components may also be varied in order to increase the stability ofPt(IV)M compounds and/or Pt(IV)M conjugates in the buffer solution overa period of time and/or under a variety of conditions.

The present invention provides for devices which may incorporate Pt(IV)Mcompounds and/or Pt(IV)M conjugates of the present invention. Thesedevices contain in a stable formulation available to be immediatelydelivered to a subject in need thereof, such as a human patient. In someembodiments, the subject has cancer.

Non-limiting examples of the devices include a pump, a catheter, aneedle, a transdermal patch, a pressurized olfactory delivery device,iontophoresis devices, multi-layered microfluidic devices. The devicesmay be employed to deliver Pt(IV)M compounds and/or Pt(IV)M conjugatesof the present invention according to single, multi- or split-dosingregiments. The devices may be employed to deliver Pt(IV)M compoundsand/or Pt(IV)M conjugates of the present invention across biologicaltissue, intradermal, subcutaneously, or intramuscularly. More examplesof devices suitable for delivering Pt(IV)M compounds and/or Pt(IV)Mconjugates include but not limited to a medical device for intravesicaldrug delivery disclosed in International Publication WO 2014036555, aglass bottle made of type I glass disclosed in US Publication No.20080108697, a drug-eluting device comprising a film made of adegradable polymer and an active agent as disclosed in US PublicationNo. 20140308336, an infusion device having an injection micropump, or acontainer containing a pharmaceutically stable preparation of an activeagent as disclosed in U.S. Pat. No. 5,716,988, an implantable devicecomprising a reservoir and a channeled member in fluid communicationwith the reservoir the as disclosed in International Publication WO2015023557, a hollow-fibre-based biocompatible drug delivery device withone or more layers as disclosed in US Publication No. 20090220612, animplantable device for drug delivery including an elongated, flexibledevice having a housing defining a reservoir that contains a drug insolid or semi-solid form as disclosed in International Publication WO2013170069, a bioresorbable implant device disclosed in U.S. Pat. No.7,326,421, contents of each of which are incorporated herein byreference in their entirety.

It will be appreciated that the following examples are intended toillustrate but not to limit the present invention. Various otherexamples and modifications of the foregoing description and exampleswill be apparent to a person skilled in the art after reading thedisclosure without departing from the spirit and scope of the invention,and it is intended that all such examples or modifications be includedwithin the scope of the appended claims. All publications and patentsreferenced herein are hereby incorporated by reference in theirentirety.

EXAMPLES Example 1: Description of HPLC Analytical Methods

Analysis of the Products by C18 Reverse Phase HPLC (Method A)

The HPLC analysis was carried out on SunFire™ C18 reverse phase column(4.6×50 mm, 3.5 μm) (Waters Corp., Millford, Mass.) with a mobile phaseconsisting of water +0.01% TFA (solvent A) and acetonitrile +0.01%trifluoroacetic acid (TFA) (solvent B) at a flow rate of 2.0 mL/minuteand column temperature of 50° C. The injection volume was 10 μL and theanalyte was detected using UV at 220 and 254 nm. The initial gradientwas 5% solvent B, increased to 95% solvent B within 1.4 minutes, thenmaintained at 95% solvent B for 1.6 minutes. All solvents were HPLCgrade.

Analysis of the Product by C18 Reverse Phase HPLC (RPHPLC) (Method B).

RPHPLC analysis was carried out on Zorbax® Eclipse XDB-C18 reverse phasecolumn (4.6×100 mm, 3.5 μm, Agilent PN: 961967-902, AgilentTechnologies, Santa Clara, Calif.) with a mobile phase consisting ofwater +0.1% TFA (solvent A) and acetonitrile +0.1% TFA (solvent B) at aflow rate of 1.5 mL/minute and column temperature of 35° C. Theinjection volume was 10 μL and the analyte was detected using UV at 220and 254 nm. The initial gradient was 5% solvent B, increased to 95%solvent B within 6 minutes, and maintained at 95% solvent B for 2minutes, then returned to 5% solvent B and maintained for 2 minutes.

Example 2: Synthesis of acetate 6-(2,5-dioxo-2H-pyrrol-1(5H)-yl)hexanoate oxaliplatin

Hydroxy (acetoxy) oxaliplatin (150 mg, 0.317 mmol, 1.0 equiv),6-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanoic acid (73.6 mg, 0.349mmol, 1.10 equiv) and1-cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbeniumhexafluorophosphate (COMU®) (149 mg, 0.349 mmol, 1.10 equiv) were mixedin dimethylformamide (DMF) (6.3 mL) and N-methylmorpholine (38 μL, 0.349mmol, 1.1 equiv) was added. The reaction mixture was stirred at roomtemperature for 2 hours. The reaction was then concentrated to drynessand the residue was loaded directly onto a C18 column (30 g) elutingwith 0-30% MeCN/H₂O gradient over 15 minutes. Fractions containing theproduct were concentrated on a rotavap before the residue was trituratedin CH₂Cl₂ and methyl tert-butyl ether TBME, yielding a yellow solid. Theproduct was re-submitted to purification using a silica gel column (4g), eluted with 0-10% MeOH/CH₂Cl₂ gradient over 15 minutes. Fractionscontaining the product were combined, concentrated, diluted withMeCN/H₂O and lyophilized to provide the product as a white solid (24.0mg, 11% yield, 97% pure); ¹H NMR (500 MHz, D₂O) δ 8.92-8.37 (m, 4H),7.01 (s, 2H), 3.46-3.41 (m, 2H), 2.92-2.80 (m, 2H), 2.37-2.29 (m, 2H),2.27-2.21 (m, 2H), 1.94 (s, 3H), 1.67-1.56 (m, 4H), 1.55-1.45 (m, 4H),1.33-1.26 (m, 2H), 1.26-1.20 (m, 2H); HPLC-MS 97%. m/z for C₂₀H₂₉N₃O₁₀Pt[(M+1)+]=667.3.

Example 3: Synthesis of a Pt(IV)M Monomaleimide, Compound 2

Step 1: Oxaliplatin (300 mg, 0.76 mmol, 1.0 equiv) was suspended inmethoxyacetic acid (3.40 g, 37.8 mmol, 50 equiv), then hydrogen peroxide(30% w/w in water, 0.13 mL, 3.8 mmol, 5.0 equiv) was added and solutionwas stirred for 1 hour. Diethyl ether was added and resultingprecipitate was filtered and dried to afford a white solid (400 mg).

Step 2: 6-maleimidohexanoic acid (126 mg, 0.596 mmol, 1.0 equiv) wassuspended in tetrahydrofuran (THF) (5 mL) then 4-methyl morpholine (65μL, 0.596 mmol, 1.0 equiv) was added followed by isobutyl chloroformate(77 μL, 0.596 mmol, 1.0 equiv). The solution was stirred at roomtemperature for 1 hour, then water (10 mL) and EtOAc (10 mL) were addedand the layers were separated. The organic layer was concentrated on arotavap to dryness. The methoxyacetate hydroxy oxaliplatin (300 mg,0.596 mmol, 1.00 equiv) was dissolved in DMF (1 mL) then activated esterwas added and solution was stirred at room temperature for 2 hours. Thecrude product was purified by reverse phase chromatography (MeCN/H₂O,0.2% AcOH) to afford the desired product, which was lyophilized,resulting in a lyophilized powder (115 mg, 28% yield). HPLC/MS (MethodA): 1.333 minutes, M+H=696.2, 697.2, 698.3.

Example 4: Synthesis of a Pt(IV)M Monomaleimide, Compound 3

Another example of a compound taught herein was synthesized startingwith oxaliplatin (1.0 g, 2.52 mmol, 1 equiv) that was dissolved inacetic acid (6 mL, 100 mmol, 40 equiv) and reacted with 30% H₂O₂ (1 mL,12.6 mmol, 5 equiv). The reaction mixture was covered with aluminiumfoil and stirred at room temperature for 24 hours. Following thisreaction, more acetic acid (3 mL, 50 mmol, 20 equiv) and 30% H₂O₂ (1 mL,12.6 mmol, 5 equiv) were added and the reaction mixture was stirred foran additional 24 hours. The suspension was filtered and the white solidresidue was washed with diethylether (Et₂O) to yieldhydroxy(acetoxy)oxaliplatin (878 mg, 74% yield, 70% pure). ¹H NMR (500MHz, DMF-d7) δ 10.42 (brs, 2H), 8.93 (m, 1H), 8.39 (brs, 1H), 7.96 (brs,1H), 7.26 (brs, 1H), 2.91-2.80 (m, 2H), 2.31-2.22 (m, 2H), 1.98 (s, 3H),1.89 (s, 3H), 1.73-1.49 (m, 4H), 1.34-1.21 (m, 2H); HPLC-MS 91%, m/z forC₁₀H₁₈N₂O₇Pt [(M+H)⁺]=474.2.

Hydroxy(acetoxy)oxaliplatin (200 mg, 0.422 mmol, 1.0 equiv) and DMF(1.10 mL) were loaded in a round bottom flask. At room temperature,isocyanate (176 mg, 0.845 mmol, 2.0 equiv) in DMF (1.0 mL) was added inone portion and the reaction was stirred at room temperature for 2hours. HPLC trace demonstrated the reaction to be completed producingalso ˜30% of bis-addition product due to the presence ofbishydroxyoxaliplatin in the starting material. Water (8.0 mL) was addedto the reaction mixture and the solution was loaded directly onto a C18column (60 g). The reaction mixture was purified using a 0-40% MeCN/H₂Ogradient over 12 column volumes. The compound eluted at 26% MeCN/H₂O.Pure fractions were combined and lyophilized to provide the product as awhite solid (157.6 mg, 55%); ¹H NMR (500 MHz, DMF-d7) δ 10.10 (s, 1H),8.92-8.63 (m, 2H), 8.35 (s, 1H), 7.07 (t, J=5.6 Hz, 1H), 7.01 (s, 2H),3.44 (t, J=7.2 Hz, 2H), 3.09-2.95 (m, 2H), 2.90-2.84 (m, 2H), 2.33 (t,J=11.4 Hz, 2H), 1.94 (s, 3H), 1.67-1.14 (m, 12H); HPLC-MS 98.6%. m/z forC₂₀H₃₀N₄O₁₀Pt [(M+1)⁺]=682.3.

Example 5: Synthesis of a Pt(IV)M Monomaleimide, Compound 4

Methoxyacetic acid (42 mg, 0.464 mmol, 1.00 equiv) was suspended in THF(3 mL) then 4-methyl morpholine (51 μL, 0.464 mmol, 1.00 equiv) wasadded followed by isobutyl chloroformate (60 μL, 0.464 mmol, 1.00equiv). The solution was stirred at room temperature for 1 hour, thenwater (5 mL) and EtOAc (5 mL) were added and the layers were separated.The organic layer was concentrated on a rotavap to dryness.Dihydroxyoxaliplatin (200 mg, 0.464 mmol, 1.00 equiv) was suspended inDMSO (4 mL) then the activated ester was added and solution was stirredat room temperature for 3 days. The remaining solid was filtered, thendiethyl ether (10 mL) was added to the filtrate and stirred for 5minutes before layers were separated. Acetone was added (20 mL) to theDMSO layer, which caused a solid to precipitate. After stirring for 5minutes, the solid was filtered, washed with acetone, and dried undervacuum to afford an off-white solid (105 mg).

2-Methoxyacetate hydroxyl oxaliplatin (105 mg, 0.21 mmol, 1.0 equiv) wasdissolved in DMF (1 mL) then 1-(5-isocyanatopentyl)-1H-pyrrole-2,5-dione(65 mg, 0.31 mmol, 1.5 equiv) was added and the solution was stirred atroom temperature for 16 hours. The crude product was purified by reversephase chromatography (MeCN/H₂O, 0.2% AcOH) to afford desired product asa lyophilized powder (67 mg). HPLC/MS (Method A): 1.203 minutes,M+H=711.2, 712.2, 713.3.

Example 6: Synthesis of a Pt(IV)M Monomaleimide, Compound 5

6-maleimidohexanoic acid (844 mg, 4.0 mmol, 2.0 equiv) anddicyclohexylcarbodiimide (DCC) (822 mg, 4.0 mmol, 2.0 equiv) werecharged in a vial and dissolved in DMF (10 mL). The solution was stirredfor 30 minutes, by which time a precipitate had formed. The solid wasfiltered, the filtrate was added to dihydroxyoxaliplatin (862 mg, 2.0mmol, 1.0 equiv) suspended in DMF (10 mL) and solution was stirred atroom temperature for 4 hours. The suspension was filtered, then ethylisocyanate (EtNCO) (206 mL, 4.0 mmol, 2.0 equiv) was added to filtrateand solution was stirred at room temperature for 30 minutes. Solvent wasthen evaporated and the residue was purified on silica gel (2-7%MeOH/DCM (dichloromethane)). Concentrated pure fractions were dissolvedin MeOH (2 mL) and added to TBME (50 mL) to afford a white precipitatethat was filtered and dried. The desired product was obtained as a whitesolid (340 mg). HPLC/MS (Method B): 3.81 minutes, M+H=695, 696, 697.

Example 7: Synthesis of a Pt(IV)M Monomaleimide, Compound 6

Hydroxy(acetoxy)(DACH)PtCl₂: (DACH)PtCl₂ (1.00 g, 2.63 mmol, 1.0 equiv)and urea hydroperoxide (UHP) (1.24 g, 13.15 mmol, 5.0 equiv) were loadedin a round bottom flask. AcOH (13 mL) and H₂O (13 mL) were added and thereaction was stirred at room temperature overnight. The yellow solutionreaction mixture was then concentrated to dryness. We noted thatstarting material was still present according to HPLC-MS traces. Thecrude solid obtained was suspended in about 10 mL of MeOH and DCM wasslowly added to obtain a suspension. After stirring for 30 minutes,filtration of the solid over a Buchner funnel provided the desiredcompound as an off-white solid (410 mg, 34.2%). HPLC-MS 93%, m/z forC₈H₁₈Cl₂N₂O₃Pt [(M+1)⁺]=457.2.

Hydroxy(acetoxy)(DACH)PtCl₂ (200 mg, 0.438 mmol, 1.0 equiv) and DMF (3.0mL) were loaded in a round bottom flask. At room temperature,1-(5-isocyanatopentyl)-1H-pyrrole-2,5-dione (273 mg, 1.31 mmol, 3.0equiv) in DMF (1.40 mL) was added in one portion and the reactionstirred at room temperature overnight. The next day, HPLC tracesdemonstrated the reaction to be completed. The reaction mixture wasloaded directly onto a C18 column (60 g) and purified using 0-60%MeCN/H₂O gradient over 15 column volumes. The compound eluted at 32%MeCN/H₂O. Pure fractions were combined and lyophilized to provide theproduct as a white solid (182 mg, 63%). ¹H NMR (500 MHz, DMF-d7) δ 10.94(s, 1H), 9.74 (s, 1H), 8.43 (s, 1H), 8.11 (s, 1H), 7.05 (t, J=6.0 Hz,1H), 7.03-7.00 (m, 2H), 3.47-3.42 (m, 2H), 3.10-2.94 (m, 2H), 2.90-2.80(m, 1H), 2.44-2.30 (m, 2H), 1.93 (s, 3H), 1.69-1.37 (m, 9H), 1.37-1.15(m, 4H); HPLC-MS 95.4%, m/z for C₁₈H₃₀Cl₂N₄O₆Pt [(M+1)⁺]=665.2.

Example 8: Synthesis of a Pt(IV)M Monomaleimide, Compound 7

6-Maleimidohexanoic acid (285 mg, 1.35 mmol, 1.00 equiv) was suspendedin THF (10 mL) then 4-methyl morpholine (148 μL, 1.35 mmol, 1.00 equiv)was added followed by isobutyl chloroformate (175 μL, 1.35 mmol, 1.00equiv). The solution was stirred at room temperature for 1 hour, thenwater (20 mL) and EtOAc (20 mL) were added and layers were separated.Dihydroxy cisplatin (450 mg, 1.35 mmol, 1.00 equiv) was suspended inDMSO (8 mL) then activated ester was added and the solution was stirredat room temperature for 3 days. Ethyl isocyanate (500 μL, 9.7 mmol, 7.0equiv) was added as a solution in DMF (2 mL) and solution was stirred atroom temperature for 1 hour. The product was purified by reverse phasechromatography (MeCN/H₂O, 0.2% AcOH) to afford the desired product as alyophilized powder (160 mg). HPLC/MS (method A): 1.473 minutes,M+H=597.1, 598.1 599.1.

Example 9: Synthesis of a Pt(IV)M Monomaleimide, Compound 8

Hydroxy(acetoxy)cisplatin was synthesized by suspending cisplatin (5.0g, 16.7 mmol, 1.0 equiv) in acetic acid (40 mL, 667 mmol, 40 equiv) andtreating with 30% H₂O₂ (6.5 mL, 83.5 mmol, 5 equiv). The reactionmixture was covered with aluminium foil and stirred at room temperaturefor 24 hours yielding a yellow solid that was filtered and washed withEt₂O to afford 2.86 g of hydroxy(acetoxy)cisplatin acetic acid complex(37% yield). ¹H NMR (500 MHz, DMSO) δ 6.57-6.10 (m, 6H), 2.33 (s, 3H),2.29 (s, 3H); HPLC-MS 100%, m/z for C₂H₁₀Cl₂N₂O₃Pt [(M+H)⁺]=377.0.

Hydroxy(acetoxy)cisplatin acetic acid complex (100 mg, 0.229 mmol, 1.00equiv) and DMF (1.0 mL) were loaded in a round bottom flask. At roomtemperature, 1-(5-isocyanatopentyl)-1H-pyrrole-2,5-dione (111 mg, 0.532mmol, 2.32 equiv) in DMF (0.8 mL) was then added in one portion andreaction stirred at room temperature overnight. Water (4.0 mL) was addedto the reaction mixture and the solution was loaded directly onto a C18column (60 g). The reaction mixture purified using a 0-80% MeCN/H₂Ogradient over 15 column volumes. The compound eluted at 30% MeCN/H₂O.Pure fractions were combined and lyophilized to provide compound 8 as awhite solid (117.0 mg, 87% yield). ¹H NMR (500 MHz, DMF-d7) δ 7.19-6.75(m, 9H), 3.45 (t, J=7.2 Hz, 2H), 3.04-2.95 (m, 2H), 1.90 (s, 3H),1.59-1.50 (m, 2H), 1.49-1.37 (m, 2H), 1.34-1.20 (m, 2H); HPLC-MS 96.7%.m/z for C₁₂H₂₂Cl₂N₄O₆Pt [(M+H)⁺]=585.2.

Example 10: Synthesis of a Pt(IV)M Monomaleimide, Compound 9

Step 1: Cisplatin (300 mg, 1.00 mmol, 1.00 equiv) was suspended inmethoxyacetic acid (4.5 g, 50 mmol, 50 equiv), then hydrogen peroxide(30% w/w in water, 0.57 mL, 5 mmol, 5.0 equiv) was added and thesolution was stirred for 2 days. Diethyl ether was then added and theresulting precipitate was filtered and dried to afford a mixture ofdimethoxyacetate cisplatin and methoxyacetate hydroxy cisplatin (1.5:1).The white solid (400 mg) was suspended in DMF (10 mL) and used forsubsequent steps. To prepare an activated ester, 6-maleimidohexanoicacid (316 mg, 1.5 mmol, 1.0 equiv) was suspended in THF (10 mL) then4-methyl morpholine (165 μL, 1.5 mmol, 1.0 equiv) was added followed byisobutyl chloroformate (194 μL, 1.5 mmol, 1.0 equiv). The solution wasstirred at room temperature for 1 hour, then water (20 mL) and EtOAc (20mL) were added and the layers were separated. The organic layer wasconcentrated on a rotavap to dryness. The resulting activated ester wasdissolved in DMF (2 mL), added to methoxyacetate hydroxy cisplatinsolution and stirred at room temperature for 2 hours then purified byreverse phase chromatography (MeCN/H₂O, 0.2% AcOH) to afford the desiredproduct as a lyophilized powder (115 mg). HPLC/MS (method A): 1.199minutes, M+H=599.0, 600.0, 601.1.

Example 11: Synthesis of a Pt(IV)M Monomaleimide, Compound 10

Step 1: Cisplatin (250 mg, 0.83 mmol, 1.00 equiv) was suspended inmethoxyacetic acid (3.75 g, 41.7 mmol, 50.0 equiv), then hydrogenperoxide (30% w/w in water, 0.47 mL, 4.17 mmol, 5.0 equiv) was added andsolution was stirred for 2 days. Diethyl ether was added and resultingprecipitate was filtered and dried to afford a mixture ofdimethoxyacetate cisplatin and methoxyacetate hydroxycisplatin (1.5:1).The white solid (350 mg) was dissolved in DMF (1 mL) then isocyanate(260 mg, 1.25 mmol, 1.50 equiv) was added and the solution was stirredat room temperature for 2 hours. Crude product was purified by reversephase chromatography (MeCN/H₂O, 0.2% AcOH) to afford desired product asa lyophilized powder (139 mg). HPLC/MS (Method A): 1.184 minutes,M+H=614.1, 615.1, 616.1.

Example 12: Synthesis of a Pt(IV)M Monomaleimide, Compound 11

To hydroxy(acetoxy)cisplatin acetic acid complex (200 mg, 0.459 mmol,1.00 equiv) suspended in DMF (0.035 M, 15 mL) was added6-maleimidohexanoic acid (130 mg, 0.61 mmol, 1.33 equiv) followed byN-methylmorpholine (67 μL, 0.61 mmol, 1.33 equiv) and COMU peptidecoupling reagent (263 mg, 0.61 mmol, 1.33 equiv). The reaction mixturewas stirred at room temperature for 15 hours. The resulting clear yellowsolution was concentrated under reduced pressure. The resulting residuewas diluted in water (20 mL) and washed twice with methyl tertiary-butylether (MTBE) (2×15 mL). The aqueous layer was concentrated under reducedpressure to an approximate residual volume of 5 mL. This solutioncontaining the product was injected onto a pre-packed C-18 cartridge (30g) and eluted on a reverse phase system with a 15-50% (MeCN/water) 15minute gradient. Pure collected fractions were combined and concentratedunder reduce pressure and residual water was removed by lyophilizationto afford compound 11 as an off-white solid (119 mg, 46%). ¹H NMR (500MHz, DMF-d₇) δ (ppm): 7.02 (s, 2H), 7.03-6.67 (m, 6H), 3.44 (t, J=7.3Hz, 2H), 2.22 (t, J=7.3 Hz, 2H), 1.90 (s, 3H), 1.57-1.46 (m, 4H),1.31-1.23 (m, 2H). HPLC-MS 99%, m/z for C₁₂H₂₁Cl₂N₃O₆Pt [(M+H)⁺]=570.2.

Example 13: Synthesis of a Pt(IV)M Monomaleimide, Compound 12

Synthesis of hydroxy(6-(2,5-dioxo-2H-pyrrol-1(5H)-yl)hexanoate)cisplatin

Cisplatin (200 mg, 0.67 mmol, 1.00 equiv) was suspended in ethanol (1mL) and was added the 6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanoicacid (703 mg, 3.33 mmol, 5.00 equiv) followed by 30% H₂O₂ (160 μL, 2.01mmol, 3.00 equiv). The reaction mixture was covered with aluminum foiland stirred at room temperature for 60 hours. The reaction mixture wasconcentrated on a rotavap to dryness, dissolved in DMF, loaded directlyonto a C18 column (30 g) and eluted with a 0-40% MeCN/H₂O gradient over15 minutes. Pure fractions were combined and lyophilized to providehydroxy(6-(2,5-dioxo-2H-pyrrol-1(5H)-yl)hexanoate)cisplatin as a yellowsolid (90.4 mg); HPLC-MS m/z for C₁₀H₁₉Cl₂N₃O₅Pt [(M+H)+]=528.2.

Synthesis of 2-(2-Methoxyethoxy)acetate6-(2,5-dioxo-2H-pyrrol-1(5H)-yl)hexanoatecisplatin

Hydroxy(6-(2,5-dioxo-2H-pyrrol-1(5H)-yl)hexanoate)cisplatin (140 mg,0.265 mmol, 1.00 equiv), 3,6-dioxaheptanoic acid (39.0 mg, 0.292 mmol,1.10 equiv) and COMU (125 mg, 0.292 mmol, 1.10 equiv) were mixed in DMF(5 mL) followed by the addition of N-methylmorpholine (32 μL, 0.29 mmol,1.1 equiv). The reaction mixture was stirred at room temperatureovernight. The reaction mixture was then diluted with water and theaqueous layer was washed with MTBE. The aqueous layer was concentratedto dryness, dissolved in water, loaded directly onto a C18 column (30 g)and eluted using a 0-30% MeCN/H₂O gradient over 15 minutes. Fractionscontaining the product were concentrated on a rotavap to dryness. Theresidue was adsorbed on silica gel and purified using a silica gelcolumn (24 g), eluted using 97-70% MeCN/H₂O gradient over 15 minutes.Fractions containing the product were concentrated, the residue wasadsorbed on silica gel and purified using a silica gel column (4 g),eluted using 0-10% MeOH/CH₂Cl₂ gradient over 15 minutes. Fractionscontaining the product were concentrated and the residue was dilutedwith MeCN/H₂O and lyophilized to provide the product, compound 12, as ayellow solid (31.8 mg, 19% yield); ¹H NMR (500 MHz, D₂O) δ 6.85 (s, 2H),4.26 (s, 2H), 3.75-3.72 (m, 2H), 3.67-3.64 (m, 2H), 3.55-3.50 (m, 2H),3.40 (s, 3H), 2.45-2.38 (m, 2H), 1.62-1.55 (m, 4H), 1.35-1.25 (m, 2H);HPLC-MS 97%. m/z for C₁₅H₂₇Cl₂N₃O₈Pt [(M+H)+]=644.2.

Example 14: Synthesis of a Pt(IV)M Monomaleimide, Compound 13

Oxaliplatin (2.05 g, 5.00 mmol, 1.00 equiv) was suspended in2-methoxyethoxyacetic acid (22.7 mL, 200 mmol, 40.0 equiv), thenhydrogen peroxide (30% w/w in water, 0.775 mL, 25 mmol, 5.0 equiv) wasadded and solution was stirred for 16 hours. MTBE (175 mL) was added andthe filtrate was decanted. The gummy residue was dissolved in DMF (5 mL)and added dropwise onto EtOAc (125 mL). The resulting precipitate wasfiltered, rinsed with EtOAc (3×20 mL) and dried under vacuum to afford awhite solid (1.75 g). HPLC/MS (method B): 2.29 minutes, M+H=547, 548,549 and 2.81 minutes, M+H=663, 664, 665. The solid consists of a 1:1mixture of desired product and bis acylation product and was used inthat composition for next step.

2-Hydroxyethyl maleimide (120 mg, 0.85 mmol, 2.00 equiv) was suspendedin THF (4.0 mL) then N-methyl morpholine (93 μL, 0.85 mmol, 2.0 equiv)was added followed by succinic anhydride (85 mg, 0.85 mmol, 2.0 equiv).The solution was stirred at room temperature for 16 hours, then N-methylmorpholine (93 μL, 0.85 mmol, 2.0 equiv) was added followed by isobutylchloroformate (110 μL, 0.85 mmol, 2.0 equiv) and the solution wasstirred at room temperature for 45 minutes. Water (10 mL) and ethylacetate (10 mL) were added and the layers were separated. Solvent wasthen evaporated, then the activated ester was dissolved in DMF andhydroxy(2-methylethoxyacetoxy)oxalplatin(IV) (233 mg, 0.43 mmol, 1.0equiv) was added and solution was stirred at 50° C. for 18 hours.Solvent was evaporated from this mixture and the crude product waspurified on silica gel (0-8% MeOH/DCM gradient) to afford the desiredproduct with residual MeOH. The residue was dissolved in MeOH (2 mL) andthe resulting solution was added to TBME (50 mL) to obtain a whiteprecipitate (compound 13) that was filtered and dried under vacuum.Compound 13 was obtained as an off-white solid (131 mg, 40% yield).HPLC/MS (method B): 3.41 minutes, M+H=771.

Example 15: Synthesis of a Pt(IV)M Monomaleimide, Compound 14

2-Hydroxyethyl maleimide (120 mg, 0.85 mmol, 2.3 equiv) was suspended inTHF (4.0 mL) then N-methyl morpholine (93 μL, 0.85 mmol, 2.3 equiv) wasadded followed to succinic anhydride (85 mg, 0.85 mmol, 2.3 equiv).Solution was stirred at room temperature for 16 hours, then N-methylmorpholine (93 μL, 0.85 mmol, 2.3 equiv) was added followed by isobutylchloroformate (110 μL, 0.85 mmol, 2.3 equiv) and solution was stirred atroom temperature for 45 minutes. Water (10 mL) and ethyl acetate (10 mL)were added and layers were separated. Solvent was evaporated, thenactivated ester was dissolved in DMF and hydroxy(acetoxy)cisplatin(IV)acetic acid complex (160 mg, 0.367 mmol, 1.00 equiv) was added andsolution was stirred at 50° C. for 18 hours. The solvent was evaporatedand crude was purified on silica gel (3-8% MeOH/DCM gradient) to affordthe desired product with residual MeOH. The residue was dissolved inMeOH (1 mL) and solution was added to TBME (50 mL) to obtain a whiteprecipitate that was filtered and dried under vacuum. Compound 14 wasobtained as an off-white solid (83 mg, 38% yield). HPLC/MS (method B):3.21 minutes, M+H=600.

Example 16: Synthesis of a Pt(IV)M Monomaleimide, Compound 15

Acetoxyoxaliplatin(4-acetylphenyl)carboxylate:Acetoxy(hydroxyl)oxaliplatin (409 mg, 0.86 mmol, 1.00 equiv),4-acetylbenzoic acid (170 mg, 1.03 mmol, 1.20 equiv) and COMU (444 mg,1.03 mmol, 1.20 equiv) were suspended in DMF (0.1 M, 8 mL) andN-methylmorpholine (114 μL, 1.03 mmol, 1.20 equiv) was added at roomtemperature. The reaction mixture was stirred at room temperature for 16hours. The reaction mixture was concentrated and the residue wassuspended on silica gel and purified by normal phase chromatographyusing a silica gel column (40 g) eluted with 5-20% MeOH/CH₂Cl₂ gradientover 15 minutes. Pure fractions were combined and concentrated in vacuumto provide the product as an off-white solid (328 mg, 61%, 94.8% pure).HPLC-MS 94.8%, m/z for C₁₉H₂₄N₂O₉Pt [(M+H)+]=620.2.

Acetate4-(1-(2-(6-(2,5-dioxo-2H-pyrrol-1(5H)-yl)hexanoyl)hydrazono)ethyl)benzoateoxaliplatin was synthesized usingacetoxyoxalplatin(4-acetylphenyl)carboxylate (328 mg, 0.529 mmol, 1.00equiv) that was dissolved in DMF (0.05 M, 10 mL) and treated with6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanehydrazide TFA salt (359mg, 1.05 mmol, 2.00 equiv). The reaction mixture was stirred at roomtemperature for 16 hours. MTBE was added to the reaction mixture until agum was formed and the solvent was decanted. To the gummy residue wasadded more MTBE and the mixture was incubated in an ultrasonic bathuntil the gum turned into a yellow solid. The solid was filtered andrinsed with MTBE to afford compound 15 (126 mg, 29%, 93.2% pure); 1H NMR(500 MHz, DMF-d7) δ 10.50 (s, 0.4H), 10.42 (s, 0.6H), 8.95-8.44 (m, 4H),7.92-7.88 (m, 4H), 7.03 (s, 0.8H), 7.02 (s, 1.2H), 3.62-3.35 (m, 6H),2.46-2.33 (m, 5H), 1.98 (s, 3H), 1.78-1.50 (m, 8H), 1.43-1.22 (m, 4H);HPLC-MS 93.2%, m/z for C29H37N5O11Pt [(M+H)+]=828.3

Example 17: Synthesis of a Pt(IV)M Monomaleimide, Compound 16

Acetoxyoxaliplatin(4-acetylphenyl)carbamate was first synthesized usingacetoxy(hydroxyl)oxaliplatin (243 mg, 0.51 mmol, 1.00 equiv) and4-acetylphenylisocyanate (124 mg, 0.77 mmol, 1.50 equiv) dissolved inDMF (0.1 M, 5 mL). The reaction mixture was stirred at room temperatureovernight. The reaction mixture was concentrated and impregnated onsilica gel. The crude product was purified by normal phasechromatography using silica gel column (40 g) eluted with 5-20%MeOH/CH₂Cl₂ gradient over 15 minutes. Pure fractions were combined andconcentrated under vacuum to provide the product as a yellow solid (241mg, 74%, 83% pure). HPLC-MS 83.1%, m/z for C₁₉H₂₅N₃O₉Pt [(M+H)+]=635.2.

Synthesis of acetate4-(1-(2-(6-(2,5-dioxo-2H-pyrrol-1(5H)-1)hexanoyl)hydrazono)ethyl) phenylcarbamate oxaliplatin

Acetoxyoxalplatin(4-acetylphenyl)carbamate (228 mg, 0.36 mmol, 1.00equiv) was dissolved in DMF (0.05 M, 7 mL) and treated with6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanehydrazide TFA salt (158mg, 0.47 mmol, 1.30 equiv). The reaction mixture was stirred at roomtemperature for 16 hours. The reaction mixture was concentrated and theresidue was triturated with acetonitrile to precipitate the product as ayellow powder. This powder was triturated first with isopropyl alcohol(iPrOH) and then with DCM to afford the desired product (70 mg, 23%,93.5% pure). HPLC-MS 93.5%, m/z for C₂₉H₃₈N₆O₁₁Pt [(M+H)+]=842.3. ¹H NMR(500 MHz, DMF-d7) δ 10.34-10.15 (m, 1H), 9.91-9.66 (m, 1H), 9.37-9.24(m, 1H), 8.88-8.66 (m, 2H), 8.59-8.48 (m, 1H), 7.80-7.73 (m, 2H),7.61-7.53 (m, 2H), 7.04-6.98 (m, 2H), 3.50-3.43 (m, 2H), 3.14-3.02 (m,1H), 2.75-2.70 (m, 1H), 2.43-2.25 (m, 6H), 2.01-1.92 (m, 3H), 1.74-1.53(m, 9H), 1.42-1.24 (m, 4H).

Example 18: Synthesis of a Pt(IV)M Monomaleimide, Compound 17

Acetoxycisplatin(4-acetylphenyl)carboxylate: Hydroxy(acetoxy)cisplatinacetic acid complex (500 mg, 1.15 mmol, 1.0 equiv), 4-acetylbenzoic acid(240 mg, 1.46 mmol, 1.27 equiv) and COMU (625 mg, 1.46 mmol, 1.27 equiv)were suspended in DMF (0.05M, 25 mL) followed by N-methylmorpholine (160μL, 1.46 mmol, 1.27 equiv) at room temperature. The reaction mixture wasstirred at room temperature overnight and the suspension slowly became ayellow solution. The HPLC-MS showed incomplete conversions, and moreCOMU (205 mg, 0.478 mmol, 0.42 equiv) and N-methylmorpholine (160 uL,1.46 mmol, 1.27 equiv) were added. The reaction mixture was then stirredfor an additional 3 hours. The reaction mixture was concentrated and theresidue was dissolved in water and purified by reversed phasechromatography using a pre-packed C18 60 g-column, eluted with 0-30%MeCN/H₂O gradient over 15 minutes. Pure fractions were combined andlyophilized to provide the product as a yellow solid (236 mg, 34%, 80%pure). The solid was triturated in MTBE to affordacetoxycisplatin(4-acetylphenyl)carboxylate (180 mg, 30% yield). HPLC-MS100%, m/z for C₁₁H₁₆Cl₂N₂O₅Pt [(M+H)⁺]=523.1.

Acetoxycisplatin(4-acetylphenyl)carboxylate (178 mg, 0.341 mmol, 1equiv) was dissolved in DMF (0.05 M, 6.8 mL) and treated with6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanehydrazide TFA salt (139mg, 0.409 mmol, 1.2 equiv). The reaction mixture was stirred at roomtemperature for 5 hours. MTBE was added to the reaction mixture until asuspension was obtained and a yellow solid was filtered to affordcompound 17 (159 mg, 64%, 97% pure). ¹H NMR (500 MHz, DMF-d7) δ 10.48(s, 0.3H), 10.40 (s, 0.6H), 7.97-7.92 (m, 2H), 7.91-7.86 (m, 2H),7.24-6.77 (m, 6H), 7.02 (s, 2H), 3.50-3.44 (m, 2H), 2.77-2.72 (m, 1.4H),2.44-2.38 (m, 0.6H), 2.40 (s, 2H), 2.37 (s, 1H), 1.94 (s, 3H), 1.73-1.64(m, 2H), 1.63-1.54 (m, 2H), 1.42-1.29 (m, 2H); HPLC-MS 98%, m/z forC₂₁H₂₉Cl₂N₅O₇Pt [(M+H)⁺]=730.2.

Example 19: Synthesis of a Pt(IV)M Monomaleimide, Compound 18

Synthesis of acetoxycisplatin(4-acetylphenyl)carbamate

Hydroxy(acetoxy)cisplatin acetic acid complex (300 mg, 0.688 mmol, 1.00equiv) was suspended in DMF (0.05 M, 16 mL) and before4-isocyanatoacetophenone (257 mg, 1.60 mmol, 2.33 equiv) was added atroom temperature. The reaction mixture was stirred at room temperatureovernight. The next morning the reaction mixture was concentrated todryness and the residue was triturated in a water and methanol mixture.The suspension was filtered and 340 mg of a yellow solid was obtainedcontaining product and 18% of a 4-acetylphenyl by-product. The solid wasdissolved in DMF and purified by reverse phase chromatography using apre-packed C18 60 g column, eluted with 0-30% MeCN/H₂O gradient over 15minutes. Pure fractions were combined and lyophilized to provide theproduct as a yellow solid (218 mg, 59% yield). HPLC-MS 100%, m/z forC₁₁H₁₇Cl₂N₃O₅Pt [(M+H)+]=538.1.

Acetoxycisplatin(4-acetylphenyl)carbamate (215 mg, 0.400 mmol, 1.0equiv) was dissolved in DMF (0.05M, 8 mL) and treated with6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanehydrazide TFA salt (163mg, 0.480 mmol, 1.2 equiv) at room temperature. The reaction mixture wasstirred at room temperature overnight. Dichloromethane was added to thereaction mixture and the suspension was filtered to provide a yellowsolid (230 mg, 77% yield, 90.9% pure). The residue obtained wastriturated with MeCN to provide compound 18 as a yellow solid (144 mg,48% yield, 97.3% pure). ¹H NMR (500 MHz, DMF-d7) δ 10.28 (s, 0.4H),10.15 (s, 0.6H), 9.74 (brs, 1H), 7.79-7.72 (m, 2H), 7.61-7.54 (m, 2H),7.22-6.81 (m, 6H), 7.02 (s, 2H), 3.50-3.44 (m, 2H), 2.74-2.70 (m, 1.2H),2.40-2.35 (m, 0.8H), 2.33 (s, 2H), 2.29 (s, 1H), 1.93 (s, 3H), 1.72-1.63(m, 2H), 1.62-1.53 (m, 2H), 1.42-1.29 (m, 2H); HPLC-MS 97%, m/z forC₂₁H₃₀Cl₂N₆O₇Pt [(M+H)+]=745.2.

Example 20: In Vitro Inhibition of Cell Proliferation by Pt(IV)MMonomaleimide Compounds

Human cancer cell lines were plated in 96 well plates (Costar) and 24hours later were treated with a compound for 48-72 hours. Specifically,H460 cells (ATCC) were plated at a concentration of 1,500 cells per welland compound treatment was carried out for 48 hours. Compound startingdose was 20 μM and three-fold serial dilutions were done for a total often points. Inhibition of cell proliferation was measured usingCellTiter-Glo® reagent using the standard protocol (Promega) and aGlomax® multi+detection system (Promega). Percent proliferationinhibition was calculated using the following formula: %inhibition=(control-treatment)/control*100. Control is defined asvehicle alone. IC₅₀ curves were generated using the nonlinear regressionanalysis (four parameter) with GraphPad Prism 6.

Selected compounds of the present teachings each has an IC₅₀ between0.0001 μM and 50 μM. For example, as shown in Table 1, some examples ofcompounds are less active than cisplatin and have IC₅₀ value greaterthan 10 μM.

TABLE 1 Compound H460 IC₅₀ (μM) Cisplatin 2.0 4 18.9 5 >500 7 40.6 914.2

These data demonstrate that some Pt(IV)M compounds described herein areweakly efficacious compared to cisplatin for inducing cell death in acancer cell under the conditions of these experiments.

Example 21: Effect of Pt(IV)M Monomaleimide Compounds on Tumor Growth

Despite the weak efficacy in vitro on cell proliferation compared tocisplatin, applicants assessed the activity of Pt(IV)M monomaleimidecompounds in vivo. In these experiments, the ability of compounds toaffect the growth of human Calu-6 NSCLC (non-small cell lung cancer)A2780 (ovarian), MIA Paca-2 (pancreatic) and BxPC-3 (pancreatic)xenografts was tested. All mice were treated in accordance with the OLAWPublic Health Service Policy on Human Care and Use of Laboratory Animalsand the ILAR Guide for the Care and Use of Laboratory Animals, and wereconducted at Charles River Laboratories (Morrisville, N.C.). All in vivostudies were conducted following the protocols approved by the CharlesRiver Institutional Animal Care and Use Committee. The MX-1 study wascarried out at TD2 (Scottsdale, Ariz.) and all procedures were carriedout under institutional guidelines of Translational Drug DevelopmentInstitutional Animal Care and Use Committee. For the A2780 in vivostudies, 10 week old female NCR nude mice were inoculated subcutaneouslyinto the right flank with 10 million cells in 1:1 RPMI 1640 (Invitrogen,Carlsbad, Calif.)/Matrigel® (BD Biosciences, San Jose, Calif.). For theCalu-6 in vivo studies, 10 week old female NCR nude mice were inoculatedsubcutaneously into the right flank with 5 million cells in 1:1 RPMI1640/Matrigel. For the MIA Paca-2, BxPC-3 in vivo studies, the tumormaterial was maintained by serial engraftment in female nude NCR nudemice. To initiate tumor growth, a 1 mm³ fragment was implantedsubcutaneously in the right flank of each test animal. The animals were9 and 10-11 weeks old at the time the study started for BxPC-3 and MIAPaca-2 models, respectively. For the MX-1 in vivo studies, tumormaterial was maintained by serial engraftment in athymic nude mice. Toinitiate tumor growth a 3×3 mm pieces implanted subcutaneously in theright flank of each test animal. The animals were 5 weeks old at thetime of implantation.

Tumor measurements were taken twice weekly, using vernier calipers.Tumor volume was calculated using the formula: V=0.5×width×width×length.

When tumors approached a volume of 100 mm³, mice were randomized intothree groups of ten animals. Mice were treated with vehicle control (10%Solutol® HS15 in saline), compound 3 or 4 at 10 mg/kg, compounds 2, 7,8, 11, 14 at 20 mg/kg, or 30 mg/kg compound 13; compound 5 was given at30 mg/kg by intravenous injection for the A2780 and Calu-6 studies.Compound 5 was dosed at 15 mg/kg for the BxPC-3 and MIA Paca-2 studies.Mice were dosed twice weekly for the duration of the study. Compound 8was dosed at 10 mg/kg and 15 mg/kg for the MX-1 study, animals weredosed twice weekly for a total of four doses. Twenty-four hours afterthe final dose tumor volumes were measured again for calculation oftumor growth inhibition. All statistical analyses were performed usingGraphPad PRISM® Version 6.00. Final tumor volumes were analyzed usingwith a one-way analysis of variance and Tukey multiple comparison test.

Efficacy data for eight compounds in the A2780 model are shown in FIGS.1-3. Table 2 shows the percent tumor growth inhibition observed in thisstudy for the eight compounds and cisplatin and oxaliplatin ascomparators. All of the tested compounds had increased inhibition oftumor growth compared to cisplatin and oxaliplatin in this model.

TABLE 2 Treatment TGI % pValue Cisplatin 54.5 p < 0.001 Oxaliplatin 45.9p < 0.001 4 57.7 p < 0.001 2 68.5 p < 0.001 7 73.3 p < 0.001 8 72.4 p <0.001 11 69.6 p < 0.001 3 74.0 p < 0.001 13 58.3 p < 0.001 14 61.7 p <0.001

Efficacy data for compound 5 in the A2780 model are shown in FIG. 4.Table 3 shows the percent tumor growth inhibition (TGI %) observed inthis study for compound 5 and cisplatin and oxaliplatin as comparators.

TABLE 3 Treatment TGI % pValue Cisplatin 44.2 p < 0.01 Oxalipiatin 40.1p < 0.05 5 84.1 p < 0.001

Efficacy data for compound 5 in the Calu-6 model are shown in FIG. 5.Table 4 shows the percent tumor growth inhibition (TGI %) observed inthis study for compound 5 and cisplatin and oxaliplatin as comparators.

TABLE 4-1 Treatment TGI % pValue Cispiatin 91.4 p < 0.001 Oxaliplatin56.7 p < 0.001 5 90.7 p < 0.001

Efficacy data for compound 5 in the BxPC-3 model are shown in FIG. 15.Table 4-2 shows the percent tumor growth inhibition (TGI %) observed inthis study for compound 5 and oxaliplatin a comparator. This pancreaticmodel is wild type for KRAS and the results of these data were directlycompared to the results seen in Table 4-3, FIG. 16.

TABLE 4-2 Treatment TGI % pValue Oxaliplatin 21.0 NS 5 47.0 NS

Efficacy data for compound 5 in the MIA Paca-2 model is shown in FIG.15. Table 6 shows the percent tumor growth inhibition (TGI %) observedin this study for compound 5 and oxaliplatin as a comparator. These datademonstrate that in the KRAS mutant pancreatic model, MIA Paca-2,compound 5 significantly inhibits tumor growth. Oxaliplatin alsodemonstrated tumor growth inhibition in this model, but to a lesserextent. The difference between the activity of Oxaliplatin and compound5 is statistically significant (P<0.05). The results demonstrate greaterefficacy of an albumin binding pro-drug vs. non-albumin binding drug inthe presence of a KRAS mutation in the in vivo setting. This datasupports the in vitro albumin uptake data, FIG. 13.

TABLE 4-3 Treatment TGI % pValue Oxaliplatin 44.0 p < 0.01 5 97.0 p <0.001

These data demonstrate that despite the weak inhibition of cellproliferation shown by compounds in vitro, surprisingly, the compoundsdemonstrated inhibition of tumor growth in xenografts equal to orgreater than that of oxaliplatin and cisplatin. It is also of note thatwhile oxaliplatin exhibited significantly different amounts ofinhibition in the two models that were tested, compound 5 was highlyeffective for inhibiting tumor growth in both models.

Example 22: Tumor Accumulation of Pt(IV)M Monomaleimide Compounds

Applicants previously disclosed two platinum-maleimide compounds (seeU.S. Ser. No. 61/922,274). The efficacy data for two maleimide compoundspreviously disclosed that they are similar to cisplatin and oxaliplatinin the A2780 model and intermediate between oxaliplatin and cisplatin inthe Calu-6 model (FIGS. 6 and 7) and are inferior in tumor growthinhibition compared to the molecules disclosed in the presentapplication. The tables below shows the percent tumor growth inhibition(TGI %) observed in these studies for compounds 19 and 20 and cisplatinand oxaliplatin as comparators.

TABLE 5 A2780 xenografts Treatment TGI % pValue Cisplatin 53.04 p <0.001 19 44.53 p < 0.001 20 56.98 p < 0.001 Oxaliplatin 43.75 p < 0.001

TABLE 6 Calu-6 xenografts Treatment TGI % pValue Cisplatin 94.57 p <0.001 19 63.57 p < 0.001 20 46.47 p < 0.05 Oxaliptatin 21.19 p > 0.05

Example 23: Tumor Platinum Levels in Tumor-Bearing Nude Mice Dosed withPt(IV)M Compounds

To examine the ability of compounds disclosed herein to accumulate intumors, a murine cancer model was used. Animals were inoculated with5×10⁵ H460 small cell lung cancer cells via subcutaneous injection tothe flank. Tumors were allowed to reach an approximate volume of ˜500mm³. Animals were then randomized into treatment groups of 3 animals pertime point and were dosed at 4 mg/kg. The 24-hour time point was used asa benchmark across compounds.

Tumor platinum levels were determined by inductively coupled plasma massspectrometry (ICP-MS). Tumors were excised from animals and dissolved infuming nitric acid (60% w/w) by adding four parts nitric acid to 1 parttumor w/w and heating overnight at 60° C. The resulting digest wasdiluted 1:10 in ICP-MS analysis buffer (1% nitric acid, 2% Triton®X-100), and directly introduced into the ICP-MS unit by peristalticpump. The end dilution factor for the samples as introduced to theICP-MS was 50×.

FIG. 8 shows the platinum levels in the tumor for 8 exemplary compoundsof the present teachings, respectively, plus cisplatin and oxaliplatinfor comparison. These data demonstrate that these compounds show higherplatinum levels in the tumors than do cisplatin and oxaliplatin. Inaddition, these data demonstrate a method of determining the ability ofa Pt(IV)M compound to deliver platinum to a tumor.

TABLE 7 Tumor platinum levels in tumor-bearing nude mice dosed withPt(IV)M compounds Platinum in tumor (mM/mmole/kg platinum Compounddosed) Oxaliplatin 0.12 Cisplatin 0.27 1 0.57 3 0.63 4 0.59 5 0.51 70.51 8 0.51 9 0.53 11  0.68

Example 24: Reaction of Compounds 5 and 8 with Albumin or Serum

Without committing to a specific mechanism, it is believed thateffective delivery of a Pt(IV)M compound is related to the covalentattachment of the compound to albumin (e.g., human serum albumin; HSA).It is estimated that Pt(IV)M compounds bind to amino acid 34 (cysteine)on an intact alumin. The circulating amount of albumin in blood is highand the covalent bonding to a Pt(IV)M compound is expected to occur inblood. The compound-albumin bond is cleaved at a tumor site, creating anactive platinum compound, e.g., a Pt(II) compound.

To confirm the ability of a Pt(IV)M compound to covalently bind toalbumin and that the reaction can occur in blood, an assay system wasused in which an HPLC system was coupled to an ICP-MS system to measurethe platinum-containing trace for albumin reacted platinum compounds. A300 angstrom pore size C18 column was run with gradient chromatographyto effect separation. The weak buffer was 10 mM pH 5 ammonium formate.The strong buffer was 90% acetonitrile and 10 mM ammonium formate. Thegradient was from 0% strong buffer to 100% strong buffer over 9 minutes.The injection volume was 5 μL of sample. Albumin containing samples weredirectly injected onto the LC-ICPMS system with no dilution, extraction,or other pretreatment.

An authentic sample of compound 5 conjugate to albumin was prepared asfollows. A 20% HSA solution was used from Lee Solutions (#R8447). Thealbumin was diluted to a concentration of 5% (50 mg/mL) with PBS. Theconjugation of compound 5 was accomplished as follows: 9 mg of 5 wasdissolved in methanol and added to 20 mL of albumin solution(concentration=50 mg/mL). The reaction was conducted for 1 hour at 37degrees C. After 1 hour, the reaction mixture was washed 25 fold withWater for Injection (WFI) by tangential filtration using a 10 KDmembrane cutoff filter (Spectrum Labs). After 500 mL of the washedfiltrate was collected, the final albumin:compound 5 conjugate solutionwas concentrated down to 16 mL. To the concentrate, 1.77 mL of 10×PBSwas added to yield an albumin conjugate solution in 1×PBS. The mixturewas sterile filtered (0.22 micron Millipore Steriflip). Theconcentration of albumin in the final solution was determined to be53.17 mg/mL. The solution was stored at 4 degrees C.

Reactions of compound 5 with serum were conducted by spiking 990 μL ofmurine serum with 10 μL of compound 5 in DMF. The resulting reactionmixture was a 1:100 dilution of drug with only 1% of solvent present inthe biological sample. The reaction was conducted at 37° C. for 30minutes prior to submission of the sample to the LC-ICPMS analysisqueue.

Control samples were reacted to determine the retention times forvarious platinum containing species. These included compound 5 andcompound 5 reacted with albumin. Following the characterization of thechromatography for retention times, rat serum was reacted with compound5 to determine the extent of reaction with albumin and the specificityof the albumin reaction. Unreacted compound 5 had a retention time of3.65 minutes (FIG. 9). Commercial human serum albumin reacted withcompound 5 had a retention time of 4.35 minutes (FIG. 10).

When compound 5 at a concentration of 300 μM was incubated in murineserum the resulting LC-ICPMS chromatogram showed 96% of the platinumsignal was observed to be albumin-bound (FIG. 11A).

Compound 8 was mixed with albumin tryptic peptide T3 and LC MS/MSanalysis was conducted. The analysis result was shown in FIG. 11B.Signals of T3 endogenous conjugates and T3-Compound 8 conjugates wereobserved and were evidence that Compound 8 binds to T3.

Example 25: Uptake of Albumin by KRAS Mutant Cells and Treating KRASMutant Tumor Cells with Compound 5

Albumin uptake was measured in BxPC3, NCI-H520, HT-29 wild type KRASexpressing cell lines and in MiaPaCa-2, NCI-H441, HCT-116 and LoVo KRASmutation expressing cell lines. As used herein, a “KRAS mutant” is acell, cell line, or tumor that harbors at least one KRAS mutation. FIG.13 showed that albumin uptake was much higher in KRAS mutant cellscompared to cells that do not harbor a KRAS mutation with the exceptionof LoVo cells. An inhibitor of macropinocytosis decreased albuminuptake.

An example of albumin uptake measurements using fluorescently labeledalbumin as an imaging agent was shown in FIG. 14. Fluorescently labeledalbumin accumulates in KRAS mutant pancreatic Mia PaCa-2 cells more thanin KRAS WT pancreatic BxPC3 cells. Radiolabelled albumin may be used asan imaging agent in humans.

The effect of Pt(IV)M monomaleimide compounds on the growth of KRASmutant and wild type expressing cells was tested using the same methodas described in Examples 21-23. Efficacy data for Compound 5 was shownin FIG. 12, FIG. 15 and FIG. 16. Compound 5 demonstrated inhibition oftumor growth greater than that of oxaliplatin in the KRAS mutant celllines, Miapaca-2 and Calu-6 as compared to the KRAS wild type line,BxPC-3. Compound 5 was highly effective for inhibiting tumor growth inKRAS mutant models Calu-6 and Miapaca-2.

Example 26: Improved Process for Synthesizing Compound 8

Preparation of compound 8 using improved procedures is presented below.

Description of the Improved Procedures for Synthesizing Compound 8Stage 1

Preparation of Hydroxy(acetoxy)cisplatin Acetic Acid Complex (Compound1′)

Cisplatin (4.93 g, 16.4 mmol, 1.00) was charged into a reactor undernitrogen atmosphere. Acetic acid (40.0 mL, 699 mmol, 42.6 eq) was addedand the resulting mixture was stirred to produce a suspension. Hydrogenperoxide 30% Wt/Wt in water (7.15 g, 63.1 mmol, 3.85 eq.) was added andstirring continued at temperatures between 23-30° C. for about 4 h(exothermic reaction). The reaction was monitored by reverse phase HPLCand stirring continued at 20-25° C. The suspension was filtered about 24h after the hydrogen peroxide addition. The cake was washed withisopropanol (3×6 mL) then with MTBE (3×6 mL). The resulting solid wasdried, in vacuo, to constant weight at 20-23° C.Hydroxy(acetoxy)cisplatin acetic acid complex was isolated as a white tooff-white powder (2.66 g, 37% yield). Purity based on HPLC>=98%. ¹H NMR(500 MHz, DMSO) δ 6.57-6.10 (m, 6H), 2.33 (s, 3H), 2.29 (s, 3H); HPLC-MS98%, m/z for C₂H₁₀Cl₂N₂O₃Pt [(M+H)⁺]=377.0.

Stage 2

Preparation of Compound 8

Hydroxy(acetoxy)cisplatin acetic acid complex (2.00 g, 4.59 mmol, 1.00eq) was charged in a reactor under nitrogen atmosphere. Anhydrous THF(20 mL) was added. The resulting mixture was stirred at 20-25° C. toproduce a suspension. Compound 2′ (Isocyanate, 2.22 g, 10.7 mmol, 2.33eq) was added as a solution in anhydrous THF (16 mL) and the reactionmixture was stirred at 20-25° C. until complete consumption of startingmaterial (as determined by reverse phase HPLC, reaction completes within14 h). The crude mixture was used immediately for the next step(precipitation/final isolation).

Compound 8 Precipitation/Final Isolation

MTBE (120 mL) was charged into a reactor under nitrogen atmosphere andstirred at 20-25° C. The crude compound 8 mixture from the previous stepwas filtered and the filtered solution was added drop-wise to thereactor containing MTBE. A precipitate readily formed when the crudecompound 8 mixture became in contact with MTBE. The equipment was rinsedwith anhydrous THF (2×2 mL). The suspension was stirred at 20-25° C. forabout 1 h. The solid was filtered and the cake washed with MTBE (3×5 mL)under nitrogen atmosphere. The cake was homogenized and the resultingpowder was dried in vacuo at 20-25° C. Compound 8 was isolated as awhite to off-white fine powder (2.58 g, 96% yield). HPLC purity>=95%. ¹HNMR (500 MHz, DMF-d7) δ 7.19-6.75 (m, 9H), 3.45 (t, J=7.2 Hz, 2H),3.04-2.95 (m, 2H), 1.90 (s, 3H), 1.59-1.50 (m, 2H), 1.49-1.37 (m, 2H),1.34-1.20 (m, 2H); HPLC-MS 96.7%. m/z for C₁₂H₂₂Cl₂N₄O₆Pt[(M+H)⁺]=585.2.

Preparation of Compound 2′ (Isocyanate)

Reaction 1

6-maleimido hexanoic acid (4.22 g, 20.0 mmol, 1.00 eq) was charged intoa reactor under nitrogen atmosphere. Anhydrous Toluene (200 mL) wasadded and the resulting mixture was stirred at 20-25° C. to obtain asuspension. Anhydrous triethylamine (3.36 mL, 24.0 mmol, 1.20 eq) wasadded. The resulting mixture was stirred at 20-25° C. until anhomogenous solution was obtained at which point DPPA (4.76 mL, 22.0mmol, 1.10 eq) was added while keeping the temperature at 20-25° C.Stirring was continued at 20-25° C. for about 5 h. NaHCO₃ 10% Wt/Wt inwater (200 mL) was added. The resulting mixture was stirred 5 min thenlayers were separated within 10 min. The organic layer was concentratedin vacuo, while keeping the temperature<35° C., until toluene (90 mL)had distilled off. Anhydrous toluene (90 mL) was added to the resultingsolution.

Reaction 2

The solution obtained from the previous step was heated to 95-105° C.for <14 h under nitrogen atmosphere. Volatiles were removed in vacuowhile keeping the temperature<35° C. Crude isocyanate was isolated as ayellow oil (4.83 g, yield=116%). The material can be used as is forpreparing compound 8. A small portion (0.4 g) was purified by silica gelchromatography for characterization purposes (purification described inthe paragraph below) and to evaluate the performance of purifiedmaterial in the compound 8 formation reaction (Stage 2, FIG. 1). Basedon LC/MS analyses of the crude reaction mixture, purified isocyanateproduced cleaner compound 8.

Purification of Compound 2′ (Isocyanate)

Silica gel purification: crude oil (0.400 g/4.83 g) was dissolved inethyl acetate/n-heptane (1:19 V/V, 2 mL) and loaded onto a Redisepcolumn (4 g, 1 CV=4.8 mL). The column was eluted with a gradient of0-50% (v/v) of ethyl acetate/n-heptane over 12 min. Targeted compoundeluted between 4.5-6.5 min. Flow rate: 18 mL/min. Fractions size: 4-6mL. Fractions were analyzed by LC/MS. Fractions containing compound 2′as a single component were combined and volatiles were removed in vacuokeeping T<30° C. Compound 2′ was isolated as a colorless oil (0.180 g).¹H NMR (500 MHz, CDCl₃) δ 6.69 (s, 2H), 3.53 (t, J=7.3 Hz, 2H), 3.29 (t,J=6.8 Hz, 2H), 1.67-1.57 (m, 4H), 1.40-1.32 (m, 2H); MS: M+1=209. TheNMR spectrum and MS data were consistent with the structure of compound2′.

Discussion

The procedures disclosed in Example 26 had two stages to transformcisplatin into compound 8. It did not involve any chromatography orlyophilization steps. Compound 8 was purified by precipitation with apurity of ≥95%. Precipitation provides superior purity (>=95% vs <95%with chromatography and/or lyophilization) and yield (85% vs 51-75% withchromatography and/or lyophilization). Purification of compound 8 byprecipitation is straightforward and conducted under conditions that:purge out impurities; provide targeted purity>=95%; prevent degradationof compound 8; provide high yields (85%). As far as cycle time isconcerned, purification of compound 8 by precipitation translates intohuge time savings: <1 day to precipitate compound 8 as a single batchand compound 8 is stable under these conditions; drastically cuts downthe number of the samples to analyze for purity. Raw material costs areminimized by a straightforward purification via precipitation because ofhigher yields. Chromatography costs are also eliminated. Furthermore,synthesis safety and safety of patients are improved. At stage 1,diethyl ether was replaced by IPA and MTBE washes. These solvents aresafe to use on large-scale. Compound 1′ was isolated with consistentlyhigh-purity>=98% with no negative impact on yield. Diethyl ether is notsuitable for scale-up due to its high-volatility, high-flammability, itstendency to form peroxides and sedative properties. Replacing diethylether by IPA and MTBE washes was found beneficial for purity and yieldof compound 1′. Isocyanate compound 2′ was purified to remove DPPA andDPPA by-products. Removal of toxic impurities such as DPPA and DPPAby-products gives higher purity isocyanate compound 2′, improves qualityof compound 8 and reduces risks for patients.

Conclusion

The method of Example 26 represents a novel path for synthesizing and/orpurifying compound 8 (targeted scale of about 0.1-about 1 Kg) because itprovides: 1) superior overall purity and yield of compound 8, 2) lesserrisk for scalability (compound 8 is more stable under purificationconditions), 3) shorter cycle-time (compound 8 is not purified by columnchromatography nor lyophilization, 4) lower raw materials costs due toimproved overall yield/removal of chromatography purification, 5) madesafer by replacing diethyl ether washes by IPA and MTBE washes, 6)rendered safer for patients by preventing impurities such as DPPA andDPPA by-products from entering in the reaction/process to generatecompound 8.

Example 27: Pt(IV)M Monomaleimide Compounds Show Increased Tumor GrowthInhibition than Cisplatin and Oxaliplatin

Pt(IV)M monomaleimide compounds (compounds 1, 3, 8 and 11) and compoundscomprising two maleimide groups (bismaleimide compounds 19, 28, 29 and30) were screened in vivo for tumor growth inhibition (TGI %) in A2780model (ovarian cancer). Cisplatin and oxaliplatin were also tested.Results in FIG. 17 showed that Pt(IV)M monomaleimide have superior TGI %to cisplatin and oxaliplatin.

Not willing to be bound to any theory, the second maleimide inbismaleimide compounds has potential to covalently link to othercysteins and lead to cross-linking or toxicity.

Example 28: Increased Platinum Accumulation and DNA PlatinationResulting in Increased Tumor Growth Inhibition than Cisplatin

Platinum levels in plasma and tumor 24 hr after a single dose ofcompound 8 at 10 mg/kg were measured in lung cancer model NCI-H460.Platinum levels in plasma and tumor at day 5 after two doses of compound8 (dosed at days 1 and 4) at 10 mg/kg were measured in lung cancer modelNCI-H520. Cisplatin was also tested. Results in FIG. 18 and FIG. 19showed that compound 8 yielded a higher platinum accumulation in bothplasma and tumor than cisplatin in both single does and two-dosestudies. Increased tumor platinum results in higher levels of DNAplatinum adducts.

Tumor growth inhibition was measured in ovarian cancer model A2780 fortreatment with compound 8 at 20 mg/kg and cisplatin. Results were shownin FIG. 20. Post-study platinum levels were also track and shown in FIG.21. The concentration of platinum in A2780 xenograph tumor tissuetreated with compound 8 was 14 fold higher than cisplatin.

Therefore, Pt(IV)M monomaleimide compound 8 provides higher platinumconcentration in tumor tissues than cisplatin and has superior efficacyin tumor inhibition compared to cisplatin.

Example 29: Pt(IV)M Monomaleimide Compounds Delivers a Sustained Amountof Platinum to Tumors

Tumor volumes and platinum levels were tracked over a course of 32 daysafter treatment of multiple doses of compound 8 (dosed at days 0, 3, 7and 10) in lung cancer (NSCLC) model NCI-H520. Compound 8 was dosed at15 mg/kg. Cisplatin was used as a compare and was dosed at 3 mg/kg. Theresults were shown in FIG. 22 and FIG. 23. Similarly high platinumlevels were observed in tumor 16 days after the last dose at day 10.Sustained release of platinum results in superior tumor growthinhibition than cisplatin.

Cell dedifferentiation and apoptosis were studied withimmunohistochemical (IHC) and TUNEL stainings. Representative imagesfrom day 10 of NCI-H520 model were shown in FIG. 24 and FIG. 25. Tumorstreated with compound 8 showed significant and sustained increase inapoptosis and dedifferentiation. These results are consistant withsuperior efficacy and platinum concentrations of compound 8 compared tocisplatin.

Example 30: Pharmacokinetics and Distribution of Pt(IV)M MonomaleimideCompounds

Platinum concentrations in rat (n=3) and dog (n=3) were both measured ina course of 100 hours and 400 hours, respectively. Cisplatin was alsotested as a compare. Results were shown in FIGS. 26 and 27. Half life ofcompound 8 in rat and dog was calculated and shown in Table 8 below.Albumin was used as a control.

Platinum exposure of compound 8 is 15-18 fold higher than cisplatin.Half-life of compound 8 parallels albumin. Therefore, Pt(IV)Mmonomaleimide compounds provide a sustained release of platinum andovercomes the rapid clearance of currently available platinum drug.

TABLE 8-1 Half-life of compound 8 and albumin in rat and dog Half-lifeRat (h) Dog (h) Compound 8 44 174 Albumin 55 211

RBC partitioning and protein partitioning were studied. Platinum in RBCand in proteins were measured after treatment with compound 8. Resultsin FIG. 28 showed that compound 8 is not sequestered in red blood cellsand 98% of compound 8 is bound to protein in plasma.

Rat PK study (N=3 rats) was carried out using compound 19 directinfusion and compound 19 pre-conjugated to albumin. Dose normalized datain FIG. 29 show there was a minimal effect on pharmacokinetics ofpre-conjugating compound 19 to albumin.

TABLE 8-2 Rat PK parameters of compound 19 direct infusion and compound19 pre- conjugated to rat albumin Pre-conjugated to Parameter UnitDirect Infusion rat albumin Dose mg/kg 2.00 2.00 Half life hr 26.8 27.3Cmax umol/L 29.3 29.2 Clearance mL/kg/min 0.09 0.13 DN AUC umol/L * hr426 407 Vss mL/kg 165 187

Example 31: A BRCA1/2 Mutant Model is Ultra-Sensitive to Pt(IV)MMonomaleimide Compounds

In vivo MX-1 human breast cancer xenograft studies were carried out withcisplatin and a Pt(IV)M monomaleimide compound. Tumor volumes of MX-1induced xenografts in mice were measured after multiple intravenousdoses of compound 8 at 15 mg/kg at day 1, day 5, day 8 and day 12 (twotimes per week for two weeks) for the main study group. Compound 8 at 10mg/kg and cisplatin at 3 mg/kg were also tested with the same dosingdays. MX-1 cell line is estrogen receptor negative and Her2 normal. Itis BRCA1 and BRCA2 mutant: BRCA1 truncating mutation (3363delGAAA) andBRCA2 mutations (16864A>C, Asn289His, and 22184A>G, Asn991Asp).Satellite groups (n=5) were collected on Day 9 for platinum tumormeasurements. Average tumor volumes and platinum levels in the tumorswere shown in FIG. 30. Tumor disappeared at day 12 after treatment withcompound 8. Additionally, no tumor regrowth was observed for the 15mg/kg group at end of study, Day 75 which was also seen with thecisplatin treated group. Only one tumor from the 10 mg/kg group began togrow back at on Day 71, with a volume of 39 mm³ at end of study, Day 75.Compound 8 also delivered higher concentrations of platinum to the tumorthan cisplatin.

TABLE 10 TGI % at Day 12 Treatment TGI % pValue Cisplatin (3 mg/kg) 95.1p < 0.05 Comound 8 (10 mg/kg) 91.3 p < 0.05 Compound 8 (15 mg/kg) 93.3 p< 0.05

Example 32: Rat Toxicology Studies for Pt(IV)M Monomaleimide Compounds

Compound 8 was evaluated in a rat toxicology study. Tubular necrosisvalues were shown in Table 11. Creatinine and urea nitrogen levels wereshown in FIG. 31. Blood markers and histopathology showed an improvementin kidney toxicity compared to cisplatin at a higher dose of platinum.No other histopathology findings of compound 8 were observed.

TABLE 11 Kidney histopathology of cisplatin and compound 8 Dose(umol/kg) Tubular necrosis Cisplatin 23 2.3 Compound 8 17 0 Compound 834 1.3

Example 33: Effect of Pt(IV)M Monomaleimide Compounds on ColorectalTumor Growth in Vitro and In Vivo

A colorectal cancer cell line, e.g., HCT-15, LoVo, SW48, SW480, HCT 116,HT115, HT29, HCA-7, etc., is plated in 96 well plates (Costar) and 24hours later are treated with Compound 5 for 48-72 hours. Compound 5starting dose is 20 μM and three-fold serial dilutions are done for atotal of ten points. Inhibition of cell proliferation is measured usingCellTiter-Glo® reagent using the standard protocol (Promega) and aGlomax® multi+detection system (Promega). Percent proliferationinhibition is calculated using the following formula: %inhibition=(control-treatment)/control*100. Control is defined asvehicle alone.

The ability of compound 5 to affect the growth of human colorectalcancer and colorectal cancer xenografts is tested. All mice are treatedin accordance with the OLAW Public Health Service Policy on Human Careand Use of Laboratory Animals and the ILAR Guide for the Care and Use ofLaboratory Animals. All in vivo studies are conducted following theprotocols approved by the Charles River Institutional Animal Care andUse Committee. Colorectal cancer is induced in 10 week old mice. Whentumors approach a volume of 100 mm³, mice are randomized into threegroups of ten animals. Mice are treated with vehicle control (10%Solutol® HS15 in saline) or compound 5 at a dose of 10 mg/kg-30 mg/kg byintravenous injection. Mice are dosed twice weekly for the duration ofthe study. Twenty-four hours after the final dose tumor volumes aremeasured again for calculation of tumor growth inhibition. Allstatistical analyses are performed using GraphPad PRISM® Version 6.00.Final tumor volumes are analyzed using with a one-way analysis ofvariance and Tukey multiple comparison test. It is observed thatcompound 5 inhibited tumor growth.

EQUIVALENTS AND SCOPE

While several embodiments of the present teachings have been describedand illustrated herein, those of ordinary skill in the art will readilyenvision a variety of other means and/or structures for performing thefunctions and/or obtaining the results and/or one or more of theadvantages described herein, and each of such variations and/ormodifications is deemed to be within the scope of the present teachings.More generally, those skilled in the art will appreciate that allparameters, dimensions, materials, and configurations described hereinare meant to be exemplary and that the actual parameters, dimensions,materials, and/or configurations will depend upon the specificapplication or applications for which the teachings of the presentteachings is/are used. Those skilled in the art will recognize, or beable to ascertain using no more than routine experimentation, manyequivalents to the specific embodiments of the present teachingsdescribed herein.

It is, therefore, to be understood that the foregoing embodiments arepresented by way of example only and that, within the scope of theappended claims and equivalents thereto, the present teachings may bepracticed otherwise than as specifically described and claimed. Thepresent teachings are directed to each individual feature and/or methoddescribed herein. In addition, any combination of two or more suchfeatures and/or methods, if such features and/or methods are notmutually inconsistent, is included within the scope of the presentteachings.

The scope of the present invention is not intended to be limited to theabove Description, but rather is as set forth in the appended claims.

In the claims, articles such as “a,” “an,” and “the” may mean one ormore than one unless indicated to the contrary or otherwise evident fromthe context. Claims or descriptions that include “or” between one ormore members of a group are considered satisfied if one, more than one,or all of the group members are present in, employed in, or otherwiserelevant to a given product or process unless indicated to the contraryor otherwise evident from the context. The invention includesembodiments in which exactly one member of the group is present in,employed in, or otherwise relevant to a given product or process. Theinvention includes embodiments in which more than one, or all of thegroup members are present in, employed in, or otherwise relevant to agiven product or process.

It is also noted that the term “comprising” is intended to be open andpermits but does not require the inclusion of additional elements orsteps. When the term “comprising” is used herein, the term “consistingof” is thus also encompassed and disclosed.

Where ranges are given, endpoints are included. Furthermore, it is to beunderstood that unless otherwise indicated or otherwise evident from thecontext and understanding of one of ordinary skill in the art, valuesthat are expressed as ranges can assume any specific value or subrangewithin the stated ranges in different embodiments of the invention, tothe tenth of the unit of the lower limit of the range, unless thecontext clearly dictates otherwise.

In addition, it is to be understood that any particular embodiment ofthe present invention that falls within the prior art may be explicitlyexcluded from any one or more of the claims. Since such embodiments aredeemed to be known to one of ordinary skill in the art, they may beexcluded even if the exclusion is not set forth explicitly herein. Anyparticular embodiment of the compositions of the invention can beexcluded from any one or more claims, for any reason, whether or notrelated to the existence of prior art.

All cited sources, for example, references, publications, databases,database entries, and art cited herein, are incorporated into thisapplication by reference, even if not expressly stated in the citation.In case of conflicting statements of a cited source and the instantapplication, the statement in the instant application shall control.

Section and table headings are not intended to be limiting.

What is claimed is:
 1. A method of inhibiting growth of a tumorcomprising contacting the tumor with an effective amount of a compoundof Formula I:

or a pharmaceutically acceptable salt thereof, wherein: X and Y areindependently selected from NH, alkyl and aryl; R¹ and R² each is Cl, orR¹ and R² are joined to form an oxalate; R³ is hydrogen, alkyl,cycloalkyl, heterocyclyl, aryl, and heteroaryl, wherein each of thealkyl, alkenyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl groupsoptionally is substituted with one or more groups, each independentlyselected from halogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl,ether, alkoxy, aryloxy, amino, amide, carbamate, alkyl, alkenyl,alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl, heterocyclyl, whereineach of the carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide,carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, or heterocyclyl is optionally substituted with one or moregroups, each independently selected from halogen, cyano, nitro,hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide,carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl, R⁴ and R⁵ are each H or together constitute acyclohexyl ring, Z is alternatively absent, alkyl, aryl, cycloalkyl,heterocyclyl, aryl, and heteroaryl, wherein each of the alkyl, alkenyl,cycloalkyl, heterocyclyl, aryl, and heteroaryl groups optionally issubstituted with one or more groups, each independently selected fromhalogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, heterocyclyl, or alkylidene hydrazinewherein each of the carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino,amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl,heteroaryl, heterocyclyl or alkylidene hydrazine is optionallysubstituted with one or more groups, each independently selected fromhalogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy,aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl,arylalkyl, cycloalkyl, heteroaryl, heterocyclyl, R⁶ is a suitablereacting group for reacting with a functional group on a protein,engineered protein, antibody, antibody fragment, peptide, agonist,antagonist, aptamer or ligand which may be capable of recognizing aselected target cell population, and/or derivatives/analogs/mimicsthereof, and wherein R⁶ is selected from an activated disulfide group, avinylcarbonyl group, a vinyl acetylene group, an aziridine group, anacetylene group or any of the following groups:

where R⁷ is Cl, Br, F, mesylate, tosylate, O-(4-nitrophenyl),O-pentafluorophenyl, and wherein optionally the activated disulfidegroup, the vinylcarbonyl group, the vinyl acetylene group, the aziridinegroup, the acetylene group may be substituted.
 2. The method of claim 1,wherein the tumor is selected from the group consisting of lung cancer,breast cancer, colorectal cancer, colon cancer, ovarian cancer,pancreatic cancer, bladder cancer, prostate cancer, cervical cancer,renal cancer, leukemia, central nervous system cancers, myeloma,melanoma, mesothelioma, stomach cancer, rectal cancer, cancer of thelarge intestine, cancer of the small intestine, esophageal cancer,uterine cancer, head and neck cancer, endometrial cancer, eye cancer,thyroid cancer, testicular cancer, bile duct cancer, liver cancer,kidney cancer, pituitary cancer, lymphoma, brain cancer, glioma,glioblastoma multiforme, meningioma, medulloblastoma, astrocytoma,neuroblastoma, basal cell carcinoma of the skin, sarcoma, synovialsarcoma, rhabdomyosarcoma, leiomyosarcoma, chondrosarcoma, andfibrosarcoma.
 3. The method of claim 2, wherein the lung cancer is asmall cell lung cancer, non-small cell lung cancer, or squamous celllung cancer.
 4. The method of claim 2, wherein the tumor is selectedfrom non-small cell lung cancer, ovarian cancer, breast cancer,pancreatic cancer or colorectal cancer.
 5. The method of claim 1,wherein the tumor has KRAS mutant cells.
 6. The method of claim 5,wherein the KRAS mutant cells have at least one homozygous KRASmutation.
 7. The method of claim 1, wherein the tumor volume is reduced.8. The method of claim 1, wherein the percent tumor growth inhibition(TGI %) is at least 40%, 50%, 60%, 70%, 80%, or 90%.
 9. The method ofclaim 1, wherein the platinum level in the tumor delivered by thecompound is at least 0.50 mM/mmole/kg platinum dosed.
 10. The method ofclaim 1, wherein the conjugation between R⁶ and the functional grouptakes place in vivo.
 11. The method of claim 1, wherein the conjugationbetween R⁶ and the functional group is performed prior to administrationin vivo.
 12. The method of claim 1, wherein the protein is albumin. 13.The method of claim 1, wherein R6 is a maleimide group and the compoundhas Formula II:


14. The method of claim 13, wherein the compound has Formula IIa:


15. The method of claim 13, wherein the compound has Formula IIb:


16. The method of claim 13, wherein R¹ and R² each is Cl.
 17. The methodof claim 13, wherein R¹ and R² are joined to form an oxalate.
 18. Themethod of claim 13, wherein R³ is alkyl.
 19. The method of claim 18,wherein R³ is methyl or ethyl.
 20. The method of claim 1, wherein thecompound is selected from the group consisting of: